MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-11-26 for STERRAD? 100NX STERILIZER 1-DR 10104 manufactured by Advanced Sterilization Products.
Report Number | 2084725-2019-00999 |
MDR Report Key | 9377522 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-11-26 |
Date of Report | 2019-11-06 |
Date of Event | 2019-11-06 |
Date Mfgr Received | 2019-11-06 |
Device Manufacturer Date | 2008-10-10 |
Date Added to Maude | 2019-11-26 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. GABRIELA MCLELLAN |
Manufacturer Street | 33 TECHNOLOGY DRIVE |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal | 92618 |
Manufacturer Phone | 949453-639 |
Manufacturer G1 | ADVANCED STERILIZATION PRODUCTS |
Manufacturer Street | 33 TECHNOLOGY DRIVE |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal Code | 92618 |
Single Use | 3 |
Remedial Action | NO |
Previous Use Code | 3 |
Removal Correction Number | Z-1026-1027-2013 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | STERRAD? 100NX STERILIZER 1-DR |
Generic Name | STERRAD? EQUIPMENT |
Product Code | MLR |
Date Received | 2019-11-26 |
Catalog Number | 10104 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ADVANCED STERILIZATION PRODUCTS |
Manufacturer Address | 33 TECHNOLOGY DRIVE IRVINE CA 92618 US 92618 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-26 |