Battery Charger: Must be built in battery charger, rectifier type with transformer, circuit breaker and overload
protection plugs into any 220VAC outlet.
Steering: A pallet truck style steer handle for easy maneuverability.
Wheels: approx. 5″ phenolic rear casters for steering and approx. 4″ phenolic wheels with roller bearings situated
from the straddle legs.
Brake: A hand controlled floor lock brake that secures the till in place.
Characteristics:
Load capacity: approx 1,500 Ibs
Load centre: approx 24 inch
Raised fork height: to match customer needs
Overall mast height: to match customer needs
Lowered height: minimum 4.0 in.
Fixed fork width: approx 7 inch
Fork length: approx 42 inch
Platform of approx. 25″ x 25″
Overall width approx 25 inch
Castors: approx 5 inch phenolic
Front wheel: approx 4 inch phenolic
(G)Technical Specification of Spore tester
Features and Specifications
it’s an Auto-reader for Bacillus Stearothermophilus to check the spore in the discharge after treatment
(Sterilization) of the waste.
Should be quite a Accurate, dependable and easy-to –use units for studying Rapid Readout Biological Indicators (RRBI)
for Steam Sterilizer
Automatically reads index outcomes.
There should be a red plus (+) light to signify sterilization failure and a green negative (-) light to verify
the sterilization conditions are met.
Available alarm in case of positive detected and RRBI is removed from the reader before final results have been
detected.
There should also be a Buzzer alarm OFF button.
The unit should be maintenance-free equipment and there shouldn’t be any light bulbs to replace for maintenance.
At least 12 Incubation/reader wells
A crushing well
Digital screen
A Press-button by pressing that, the incubation time remaining for each individual incubation/reader well that
contains a RRBI will be displayed.
Power: 220 VAC, 50Hz
Accessories to be included
Samples/kits-100 pcs
Documents to be filed as follows-
Fabricators accreditations
Test Report to prove ZERO harmful emission level provided as samples from other installations
Test report to demonstrate sterility achieved at 6log10 degree to be given upon commissioning report and validation
Technical proposal should include:
The hospital should offer the essential space; construction & infrastructure; Sufficient Power, steam supply and
connection up to space; water & Sewage line to the space.
Room Preparation: Preparation, Renovation & Modification of this room is providers responsibility
The supplier should submit the essential drawing(s) showing space requirement (room size (L x W x H ), dimensions
of chips & ancillary equipment.
Provider must give the suggestion of the complete power requirement of the entire until and on the hospital will
ensure the power supply. However, connections within the room is providers responsibility
The connection/fittings from the chip and ancillary equipment to sewage and water line is providers
duty
A detailed training proposal including the term of staff training on how to operate and take care of the processor.
A detailed maintenance schedule.
List of Spare components and accessories required for maintenance of this system
Warranty & After Sales Services:
Warranty period will be minimal 03 (three) years or as offered by the manufacturer which comes later.
Warranty period will be counted from the date of handing over of machine to the consumer in working condition i.e.
date of commission
In warranty period the supplier need to offer all maintenance & repair services.
Brach time won’t be counted in warranty period.
At last 10 year ago up services (including warranty period ) has to be ensured by the supplier.
The repair/maintenance work should be carried out within 72 hours after getting request for such from the consumer.
Quality Standard: CE/FDA certification of the offered item must be filed with the offer
For confirmation of this certification bidder must submit the followings:-
I)Mailing Address of the issuer of this certificate
ii)Web-site, email address & Fax & Telephone Number of the issuer
The bid will be non-responsive if:-
I)The certificate cannot be reached
ii)The issuer fails to authentic the certification within the bid validity
iii)The issuer confirms that the submitted certification is faulty in terms of authenticity or validity.
Failure to establish the authenticity of the certification the bidder is liable to render the bid non-responsive and
the bidder open to act in the line with applicable regulations and act.
oOriginal catalogue has to be filed
oOriginal information sheet must be submitted.
iii)The issuer confirms that the submitted certificate is defective in terms of authenticity or validity.
Failure to establish the authenticity of the certificate the bidder is liable to render the bid non-responsive and
the bidder open to action in the line with applicable regulations and act.
oOriginal catalogue must be submitted
oOriginal data sheet must be submitted.
