Technical Specifications for Duodenoscope, Video, Flexible
Annex A – Duodenoscope, Video, Flexible
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Annex A
Technical Specifications for Duodenoscope, Video, Flexible
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Dec 2012Page 1 of 1
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Contractor Stamps and Authorised Signature
Annex A – Duodenoscope, Video, Flexible
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Technical Specifications for Duodenoscope, Video, Flexible
1.Functional Requirements.
1.1The duodenovideoscope is intended for use with a compatible video endoscopy system(Fujinon,Olympus and Pentax,etc)to provide visual diagnosis, treatment, and documentation of diseases of the duodenum by ERCP(Endoscopic Retrograde Cholangiopancreatography) procedures.
1.2The duodenovideoscope shall have the capability for side viewing.
2.General Requirements
2.1 The duodenovideoscope shall be designed with a single charge-couple-device (CCD).
video system for providing high-resolution images and shall form an integral component of the duodenovideoscope.
2.2 The weight of the duodenovideoscope supported by the endoscopist during a procedure (working weight) shall be as small as possible.
2.3 The outer diameter of any portion of the duodenovideoscope that enters the patient should be thin and shall be within 1.0mm of the manufacturer specified value.
2.4 The duodenovideoscope flexibility shall be graded along its insertion tube; it should be highest at the distal tip and lowest at the proximal end of the insertion tube.
2.5 The insertion depth markings on the duodenovideoscope shall not be more than 10cm apart and shall be accurate to within 2.0mm per 10cm and within 1.0cm in overall length.
2.6 The insertion depth markings shall be clearly readable at a glance from any viewing angle.
2.7 The turning directions of the angulation control knob on the duodenovideoscope head shall be logical and correspond with directions marked on the knob and with the deflection of the distal tip.
2.8 The force required to insert manufacturer-supplied instruments through the instrument channel of the duodenovideoscope shall be as small as possible, even during coiling of the insertion tube and deflection of the distal tip.
2.9Cleaning the duodenoscope lens shall be fast and effective. It shall be easy to fill and verify the level of water in the water bottle.
2.10The entire duodenovideoscope including its air, water, carbon dioxide and instrument (suction/biopsy) channels shall be designed so that all internal surfaces can be manually cleaned using a brush.
2.11The duodenovideoscope shall be supplied with the appropriate hardware (i.e the reprocessing adapters) and a required procedure for effective cleaning and disinfection and sterilization.
2.12The duodenovideoscope shall allow adequate fluid flow through each channel, which can be verified during reprocessing, and exposure of all surfaces to the reprocessing liquids. For this matter, the tenderer must ensure that the Gastrointestinal videoscope fit into our existing Olympus or Evotech or Steris Endoscope Washer.
2.13An effective leak-testing device and procedure shall be provided with the duodenovideoscope.
2.14The duodenovideoscope shall be suitable for use in the local climatic conditions.
2.15 The duodenovideoscopeshall be adaptable to the commercially available video camera system(Fujinon,Olympus and Pentax,etc) and light source.
3.Technical Requirements
3.1The Contractor shall furnish full technical specifications for the complete system.
3.2 Working weight: 700 gm
3.3 Field of view : 100
3.4 Direction of view: 5retro (side viewing)
3.5 Depth of field: 5 - 60 mm
3.6 Distal end outer diameter: 13.5 mm
3.7 Insetion Tube outer diameter: 11.3 mm
3.8 Bending Section
a) Range of tip bending: Up 120 Right 110
Down 90 Left 90
3.9 Working length: 1240 mm
3.10Instrument Channel Inner diameter : 4.2 mm
3.11Biopsy Forceps
a)minimum visible distance: 10 mm from objective lens surface
3.12Total length: 1550 mm
4.Standards
4.1The system shall fully conform to the following:
a.IEC / EN 60601-1, General safety requirements for medical electrical equipment.
b.IEC / EN 60601-1-2, Standard for Electromagnetic Compatibility – Requirements and tests
c.IEC / EN 61000-4-x series safety requirements and tests for Electromagnetic Compatibility, Immunity
d.IEC / EN 60529 (1989), Degrees of protection provided by enclosures (IP code)
e.International available standards in the particular requirements for safety and performance for the tendered Article
f.FDA clearance
4.2Contractors have to comply with Health Science Authority (HSA) Medical Device Regulation requirements for all classes of medical devices. A copy of the HSA registration certificate must be submitted together with the tender submission.
5.Standard Accessories
5.1All standard accessories required for the normal operation, shall be listed with itemised prices and included in the unit base price.
5.2All standard accessories shall include the following items :
a. Instrument case
b.Channel cleaning brush x 1
c. Biliary Drainage tube set x 1
d. Channel cleaning adaptor x 1
e. All Channel irrigator x 1
f. Lens cleaner x 1
g.Semi disposal Biopsy valves x 10
h. Lubricant x 1
i.Water resistant cap x 1
j.Cannula with stylet x 1
k.Forceps raiser cleaning attachment x 1
l.Stopcock x 1
m.Mouthpiece x 2
n.Biopsy (fenestrated) forcep x 1
o.videoscope cable attachment to our existing Endoscopy video system.
p.All other accessories, connectors and adaptors for the smooth operation of the unit.
6.Optional Accessories
6.1The optional accessories and consumables available with the unit shall be quoted separately with itemized price.
7.Installation / Commissioning Requirements
7.1The Contractor shall inspect the site and fully acquaint himself with the nature of the work and the local conditions and facilities available, including water, drainage, ventilation and air-conditioning, where the Article is to be installed, before submitting his tender. He should also utilise other means he may prefer or consider necessary in order to fully ascertain other matters, site accessibility to equipment, conditions or constructions that may have a bearing on, or in any way affect the preparation of his tender. No claim for extra payment will be entertained by the Hospital owing to the Contractor’s neglect in this regard and any unforeseen difficulties for which provision is not made. This will in no way relieve the Contractor from the full execution of all works necessary to complete the installation. A Contractor, by the fact of submission of a tender, shall be deemed to have accepted all conditions and stipulations of this clause, which shall be binding on the Contractor.
7.2For the testing & commissioning and thereafter for the warranty preventive maintenance & corrective maintenance or on service contract preventive maintenance & corrective maintenance, the contractor shall be represented by competent staff, suitably equipped with all necessary calibrated test and measuring instruments including electrical safety analyser with printout, who shall test and commission or performing the preventive maintenance the Articles in the presence of and to the satisfaction of the Company’s authorised representatives. The Contractor must perform the electrical leakage safety test for the equipment during commissioning and for every preventive maintenance servicing during warranty preventive maintenance & corrective maintenance or on service contract preventive maintenance & corrective maintenance with no cost to the hospital.( Please refer SCC.3, Clause 11 for details )
7.3The testing and commissioning of the Article shall be in accordance with clause 11 of *SCC.3 called under Material Management Department. No payment shall be made if any of the stated requirements under this clause were not met. Notwithstanding the incomplete acceptance of the Article, the Company has the right to utilise the Article while waiting for any incomplete supply , measurements , testing and training to be delivered.
7.4All mains operated electrical Articles shall be complete with suitably insulated and sheathed three-core hospital grade flexible power cords of voltage and current rating appropriate to the Articles. Article for operating theatre shall be supplied with flexible power cords each of not less than 5m length, although the exact length shall be negotiable later. The flexible power cord shall be fitted with three-pin, high impact, unbreakable nylon body electrical plug meeting BS 1363/A or equivalent. The plug shall be of good quality consistent with hospital safety, moulded construction type and shall be equivalent to “Volex V.1307W”, BICC 3583-07”, or MK Toughplug”, 13A nylon unbreakable plugs. The plug shall be wired in conformance with sub-clause 6.5 of IEC 60601-1.
7.5The successful vendor shall dismantle and remove for disposable the existing old equipment before installing the new equipment. The cost of disposal of old equipment shall be included in the tender submission. No claim for extra payment will be entertained by the Hospital owing to the disposal of old equipment.
8.Additional Requirements
8.1The supplied equipment and accessories must be of hospital-grade and shall comply with national and internationally recognised Standards and applicable Standard Systems.
8.2 The Contractor shall provide test certificates from an internationally recognised testing body attesting to compliance with recognised standards. * If certificates for the STATED compliance are not provided during the submission, it shall be considered as non-compliant to the standard.
8.3The Contractor is expected to equip with all necessary test tools and successfully commission the Article 14 days from the date of delivery. Failure of which the Company has the right to return the Article to the Contractor. No claim for payment will be entertained by the Company. A Contractor, by the fact of submission of the tender shall be deemed to have accepted all conditions and stipulations of this clause, which shall be binding on the Contractor.
8.4The testing and commissioning of the Article shall be in accordance with clause 11 of *SCC.3 called under Material Management Department. No payment shall be made if any of the stated requirements under this clause were not met. Notwithstanding the incomplete acceptance of the Article, the Company has the right to utilise the Article while waiting for any incomplete supply to be delivered.
8.5The Contractor should be a direct representative/distributor of the manufacturer for all Articles including accessories.
8.6The Contractors shall submit a letter of appointment from the manufacturer as sole agent in Singapore for the articles offered. The Contractor shall also specify:
a)The number of years that they have been appointed agent; and
b)The expiry date of the current agency agreement;
c)The expected date of discontinuation of this product.
8.7All mains operated electrical Articles shall be complete with suitably insulated and sheathed three-core hospital grade flexible power cords of voltage and current rating appropriate to the Articles. Article for operating theatre shall be supplied with flexible power cords each of not less than 5m length, although the exact length shall be negotiable later. The flexible power cord shall be fitted with three-pin, high impact, unbreakable nylon body electrical plug meeting BS 1363/A. The plug shall be of good quality consistent with hospital safety and shall be equivalent to “Volex V.1307W”, BICC 3583-07”, or MK Toughplug”, 13A nylon unbreakable plugs. The plug shall be wired in conformance with sub-clause 6.5 of IEC 60601-1.
8.8The warranty shall cover unlimited breakdown service calls, calibration and software upgrades, at no additional cost. The preventive maintenance of the unit shall be in accordance with the manufacturer's procedure and interval. The regular preventive maintenance shall include testing in compliance to IEC 60601.1. The Contractor shall at the time of submission, provide a copy of the preventive maintenancechecklist, method and procedures. The Contractor shall provide back-up units during the warranty period while the unit is undergoing corrective repair by the Contractor.
8.9In the event of equipment breakdown and the downtime exceeds 24 hours, the Contractor shall be responsible for arranging a loan unit of similar capacity to be used by the Company. All cost shall be borne by the Contractor.
8.10The successful Contractor shall provide appropriate In-service training for Physicians, Nurses, Clinical staff, Laboratory Technologist, etc and Technical Service Training for Biomedical Engineers/Technicians. A qualified full time trainer shall conduct the training. In-service training shall be provided by qualified clinical instructors who are not sales personnel. Technical service training shall be provided by a qualified engineer. The technical service training shall be comprehensive and provided to a level such that the Company’s nominated service personnel are able to:
a.Apply or handle; and
b.Install, repair, calibrate, maintain or overhaul
all models of equipment purchased from the Contractor. The outline of the Technical service training programme must include - installation instructions; system overview with block diagram; detailed theory of operation; detailed preventive maintenance procedures; detailed calibration and performance checks; detailed trouble shooting; overhaul procedures. Full warranties for all equipment shall remain in place until at least training for the in-house engineer s has been completed. Following the completion of training, the Contractor shall, if requested, certify that trained personnel have completed the Contractor’s training program.
All In-service and technical service training shall be dedicated to the Company and conducted at the Company’s facilities unless otherwise agreed upon. The Contractor at the point of training shall provide the Article. All cost shall be borne by the Contractor.
8.11The Contractor shall submit full details of system, inclusive of a complete list of options currently available and options that will be available or are currently under development.
8.12The Company will be entitled to purchase all replacement parts, components, subassemblies and peripheral devices as needed for the maintenance and repair of each model of equipment purchased from the successful Contractor at the fair market price. No excessive handling or shipping charges will be applied to these purchases. The successful Contractor must expedite all shipments and not withhold shipments in order to increase equipment downtime to the Company or for any other reasons.
8.13The Company has the right to use any service representative of his choosing, including in-house, third party or independent contractor. These representatives have the right to repair, install, calibrate, maintain or overhaul all models of equipment purchased from the successful Tender. The Company’s representatives shall be afforded the privilege of ordering all necessary repair parts and components from the successful Contractor for each model of equipment purchased at a fair market price.
8.14The Tender shall guarantee the availability and sale directly to Company or its representative of spare parts, schematics, parts lists, troubleshooting manuals, operator's instruction manuals, and all other technical data for the life of the equipment and that replacement of defective parts or other equipment maintenance by Company or its representative will not affect warranty conditions.
8.15The Company has the right to use and operate all hardware and software for the purposes of operating, repairing, or calibrating the equipment. The Company has the right to allow her designated service representative to use all software for the repair and calibration of the equipment purchased.
8.16The supply of the system computer must be from a registered computer manufacturer and be supported by the manufacturer’s service center. The model must fulfill the basic safety requirements of Radio Frequency Interference, Electromagnetic Immunity and Safety for Information Technology Equipment. Proof of safety compliance must be presented during the submission.
8.17The Company has the right to send her designated service representatives to the manufacturer’s service training school to receive sufficient, any or all, technical training to allow the representative to repair and calibrate the equipment purchased.
8.18All documentation, software and manuals become the sole property of the Company.
8.19Upon sale or transfer of the equipment purchased within and/or outside of Singapore, the Company’s shall have the right to transfer any or all hardware, software, documentation and manuals to the new purchaser of the equipment.
8.20The Contractor is advice to check for incompleteness and misleading information that may result in disqualification.
8.21All Contractors are to comply with all requirements stated in the Company Standard Conditions of Contract - *SCC.3.
8.22Failure to comply with any of the above requirements may result in the rejection of the offer.
*SCC.3 is available from Material Management Department.
All Tenderers are to acquaint themselves with the details requirements set out in SCC.3.
A. PERFORMANCE SUMMARY FOR DUODENOSCOPE, VIDEO, FLEXIBLE
Contractor/Company: ______
Description Of system/Unit: ______
Manufacturer / model: ______
Year of model 1st Sold: ______
Year of manufacture: ______
Country of origin: ______
Warranty period(Min. 2 years): ______
(The Contractor shall provide a twenty-four (24)-month warranty period, commencing from date of successful completion of commissioning. The Contractor shall replace all original parts including rechargeable battery, provide free labour with unlimited breakdown repair calls and shall also provide regular preventive maintenance as specified in the manufacturer’s latest technical manuals or operating manuals during the warranty period at no cost to the Company)
(*Please delete where applicable)
You are advised to be truthful in your submission. Nothing is to be left blank. Where compulsory submissions are required, kindly furnish as required to avoid disqualification.
A Performance Summary must accompany each option offered
No cross-referencing should be used in this performance summary unless specified by the Company.
1.FULL COMPLIANT with* Yes/No
technical specifications
2.NON-COMPLIANTpls state number only with technical specifications
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3.APPLICATIONpls specify______
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4.OVERALL SIZE, H, W, D cmpls specify
Provide a breakdown for each piece ______
of apparatus if it is not an integrated system.
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5.OVERALL WEIGHT, kgpls specify
Provide a breakdown for each piece ______
of apparatus if it is not an integrated system.
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6. TYPE (e.g Video, fiberoptic,etc)pls specify______
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7. WORKING LENGTHpls specify______
8.INSERTION TUBE,
Diameter, mmpls specify______
9. INSTRUMENT CHANNELS
Diameter, mmpls specify______
10.OPTICS
a.Field of view, degpls specify______
b. Depth of field, mmpls specify______
c. Ocular adjustmentpls specify______
d. Diopter range pls specify______
11. TIP DEFLECTION, degpls specify______
a.Up/downpls specify______
b. Right/left pls specify______
c.Maximumpls specify______
12. DISTAL TIP