Bid number 9183287 for two Shredder and sterilization devices for hazardous medical waste with installation the bid is for Egyptian companies

Specifications of shredder and sterilization devices for hazardous medical waste:

1. The devices provided must have previously obtained the approval of the Hazardous Medical Materials and Waste Committee on the technology used in them.
2. The devices imported to treat hazardous medical waste resulting from health care activities by chopping and sterilization shall be used in the country of origin for the same purpose.
3. The existence of a previous work for the same devices provided in accredited official bodies.
4. Provide evidence of the existence of an approved maintenance center for these devices within the Arab Republic of Egypt from the Industrial Control Authority.
5. The required capacity of the chopping and sterilization device in one suit has a volume of not less than (500 to 1,500 liters) per session.
6. The way the device works is in a closed cycle automatically from the beginning of the cycle to its end so that the components of the unit are sterile at the end of the sterilization cycle and the sterilization product is safe.
7. The waste was loaded into the device in one batch before the start of each cycle.
8. The cooling water and external drainage from the device must be free of any contaminants with the results of the analysis of samples outside the external drainage of the device and be in accordance with the laws and decisions within the Arab Republic of Egypt.
9. The safety of the air and drainage leaving the device must be ensured from pollutants.
10. Do not use or add chemicals or solutions during operation.
11. The device must work on a system of consecutive cycles without long intervals to prevent wasting time.
12. The device must deal with the proximity of blood.
13. The control system for all functions and programming must be automatic.
14. The device is equipped with an indicator to indicate the completion of the cycle and indicators to clarify the start of operation, pressure, temperature and end of operation, and the device can only be opened after the completion of the sterilization cycle to ensure that the waste is sterilized, and the device does so automatically.
15. The device is equipped with a printer and a recording system for the stages of the cycle.
16. The device is equipped with a unit safety alarm system in the event of a sudden failure of the unit and any increase in temperature or pressure above the permissible limit.
17. The device is equipped with an emergency program in the event of any technical failure.
18. The device includes an elevator to remove waste that is supplied within the contents of the device and within its price.
19. A sample must be taken for analysis of (sterility and heavy den) before the device is delivered initially, provided that the result of sterility is not less than 10 log6 and for 10log 4 spores.
20. Discharge the output from the device after processing automatically.
21. Output after processing: cannot be reused
22. Work system: The work is carried out in all stages of mincing and sterilization in an automated manner and human intervention is not allowed.
23. Course time: no more than 60 minutes.
24. Provide a certificate of high efficiency guarantee for the device in the event of working for a period of time up to 20 hours a day.
25. The device must have a set of filters to remove contaminants, odors and fumes from the air coming out of the device inside the room.
26. The installation site should be compatible with environmental aspects such as ventilation and the presence of a suitable solution for odors and fumes emitted when opening the gate of the sterilization unit
27. The executing company is responsible for preparing the sites to be installed and providing it with water, drainage and ceramics for the floor, walls and electricity, and the room is provided with a ventilation hole equipped with a narrow wire opening and equipped with a movable glass roll at its own expense.
28. The work of a pre-treatment room (temporary storage room for waste) as well as the work of another room after treatment (chopping product)
29. The percentage of noise and vibrations during operation shall not exceed the limits stipulated in the laws and regulations governing this matter and provide proof thereof.
30. A current stabilizer must be supplied with the device.
31. The company is committed to providing a warranty period of not less than 3 years on all parts of the body, including (drum - knives - blades - etc.) and all consumables. (With another 3-year service offer including spare parts and consumables after the end of the warranty period)
32. The company advances or the device contains within its components a special unit attached to the device to detect metal devices (Metal Detector With all metals/ stainless steel/ ferrous/discrimination programs)  Which may be located inside the hazardous medical waste bags and cannot be minced with the blades of the device so that they can be excluded from entering the device so as not to damage the blades of the chopping process.
33. Training workers on the initial rapid operation and maintenance work in case of malfunctions and providing evidence of this.
34. In the case of pressure and steam devices, the capacity of the steam generator is determined.
35. No need to use special bags to collect or sterilize the resulting waste.
36. Submit a maintenance offer after the end of the warranty period during the examination of the submitted offers.
37. Commitment to supply all original spare parts, including knife blades and any spare part in the device of the same type of device and from the same country of origin in the warranty or maintenance period.
38. A technical and financial offer of spare parts is submitted after the end of the warranty period during the examination of the submitted offers.
39. The device must have the CE certificate.
40. The device country of origin must be within European Union or USA.
41. The sterilization process must be done with using steam under pressure.