incinerator for medical waste

Lifting Chains: Must be double lifting chain of roller fashion & need to meet security factor at least 6:1.

Hydraulic System: Durable cylinder with a chrome plated ram and a relief valve for overload protection

Forks: Heavy duty steel approx. 4.0″ wide x 42″ long fixed forks

Platform: solid steel

amplifier: A heavy duty 12 volt, 125 amps/hour industrial strength battery.

Battery Charger: Must be built in battery charger, rectifier kind with transformer, circuit breaker and overload

protection plugs to any 220VAC socket.

Steering: A pallet truck design steer handle for simple maneuverability.

Brake: A hand controlled flooring lock brake that secures the until set up.


Load capacity: approx 1,500 Ibs

Load centre: approx 24 inch

Raised fork height: to suit client needs

Total mast height: to suit client demands

Lowered height: minimum 4.0 inch

Fixed fork width: approx 7 inch

Fork length: approx 42 inch

Platform of approx. 25″ x 25″

Total width approx 25 inch

Castors: approx 5 inch phenolic

Front wheel: approx 4 inch phenolic

(G)Technical Specification of Spore tester

Characteristics and Specifications

it’s an Auto-reader for Bacillus Stearothermophilus to test the spore from the release following therapy

(Sterilization) of the waste.

Should be a very Accurate, dependable and easy-to –use  units for reading Rapid Readout Biological Indicators (RRBI)

for Steam Sterilizer

Automatically reads index effects.

There ought to be a red plus (+) light to indicate sterilization failure and also a green negative (-) light to verify

that the sterilization conditions have been met.

Available alert in case of positive discovered and RRBI is removed from the reader before final results have been


The unit ought to 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 display

A Press-button by pressing that, the incubation time staying for every individual incubation/reader nicely that

includes a RRBI will be displayed.

Power: 220 VAC, 50Hz

Accessories to be contained

Samples/kits-100 pcs

Records to be submitted as follows-

Fabricators accreditations

Test Report to prove ZERO harmful emission amount provided as samples from other installations

Test report to demonstrate sterility achieved at 6log10 level to be provided upon commissioning analysis and analysis

Technical proposal should include:

The hospital must offer the necessary distance; construction & infrastructure; Sufficient Power, steam supply and

connection up to space; water & Sewage line into the space.

Room Preparation: Preparation, Renovation & Modification of the area is providers duty

The provider should submit the necessary drawing(s) displaying space requirement (room size  (L x W x H ), measurements

of processors & ancillary equipment.

Provider must give the suggestion of the entire power requirement of the whole until and on the clinic will

guarantee the energy source. But connections  inside the area is providers duty

The connection/fittings in the processor and ancillary equipment to water and sewage line is providers


A detailed training proposal involving the duration of staff training about the best way to operate and take care of the processor.

A detailed maintenance schedule.

List of Spare parts and accessories required for maintenance of the machine

Warranty & After Sales Services:

Warranty period will be minimum 03 (three) years or as offered by the producer which comes later.

Warranty period will be counted from the date of handing over of machine to the user in functioning condition i.e.

date of commission

In warranty period the provider have to offer all maintenance & repair services.

Brach timing won’t be counted in warranty period.

At last 10 year back up services (such as warranty period ) needs to be ensured by the provider.

The repair/maintenance work ought to be completed within 72 hours after getting request for this from the user.

Quality Standard: CE/FDA certification of the supplied item has to be submitted with the offer

For confirmation of the certification bidder should submit the followings:-

I)Mailing Address of the issuer of the certification

ii)Web-site, email address & Fax & Telephone Number of the issuer

The bidding will be non-responsive if:-

I)The certificate cannot be contacted

ii)The issuer fails to authentic the certification inside the bid validity

iii)The issuer verifies that the submitted certification is defective concerning credibility or validity.

Failure to establish the authenticity  of the certification the bidder is liable to leave the bidding non-responsive and

the bidder open to action in the line together with applicable regulations and behave.

oOriginal catalogue has to be submitted

oOriginal information sheet has to be submitted.

the bidder open to action in the line with applicable regulations and act.

oOriginal catalogue must be submitted

oOriginal data sheet must be submitted.


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