Equipment(UPT Immunoassay Analyzer_SR NO-SU3A20090554SEN_MODEL NO-UPT-3A-1800_HOSP-EQ-PG-25) Documents and Records^^^
| Requirement | Type and Location | Help |
|---|---|---|
| a.identity of the equipment | UPT Immunoassay Analyzer_SR NO-SU3A20090554SEN_MODEL NO-UPT-3A-1800_HOSP-EQ-PG-25 | Use Equipment Name and Hospital Register page Number to create ID. It is same as in LIS cl_general.equipment.equipment upload pdf of orders |
| b.manufacturer’s name, model and serial number or other unique identification | UPT Immunoassay Analyzer_SR NO-SU3A20090554SEN_MODEL NO-UPT-3A-1800_HOSP-EQ-PG-25 pic-1  | Unique ID of equipment in manufacturer's context |
| c.contact information for the supplier or the manufacturer | ????????? | Address, company/local sale/engineer phone/email, number for automated complaint registration etc |
| d.date of receiving and date of entering into service | 12-09-2021 | Same as in register |
| e.location | Clinical Biochemistry lab | Lab section/room etc |
| f.condition when received (e.g. new, used or reconditioned) | New | |
| g.manufacturer’s instructions | guideline_il-6.pdf | User manual pdf |
| h.Procedural document for and records that confirmed the equipment’s initial acceptability for use when equipment is incorporated in the laboratory | it was received in biochemistry lab on 12-9-2020 and after receiving we opened instrument and seen all parts of the machine and attached wire seen that it is working il-6_calibration_certi.pdf | It may be in user manual. In that case write chapter/page numbers for easy reference |
| i.Record of maintenance carried out and the Procedural(schedule) document for preventive maintenance | ||
| j.Procedural document and records that confirm the equipment’s ongoing acceptability for use;Such records include copies of reports/certificates of all calibrations and/or verifications | ||
| k.Documented Procedure for repair and Records of damage to, or malfunction, modification, or repair of the equipment |