MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-30 for HETTICH EBA 21 1004 manufactured by Andreas Hettich Gmbh & Co. Kg.
Report Number | 3005990076-2020-00002 |
MDR Report Key | 9647956 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-01-30 |
Date of Report | 2020-01-30 |
Date of Event | 2018-11-29 |
Report Date | 2018-12-10 |
Date Reported to Mfgr | 2018-12-10 |
Date Mfgr Received | 2018-12-10 |
Device Manufacturer Date | 2014-02-24 |
Date Added to Maude | 2020-01-30 |
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 | MR. JOHANN GIEBELHAUS |
Manufacturer Street | FOEHRENSTR. 12 |
Manufacturer City | TUTTLINGEN, BADEN-WUERTTEMBERG 78532 |
Manufacturer Country | GM |
Manufacturer Postal | 78532 |
Manufacturer G1 | ANDREAS HETTICH GMBH & CO. KG |
Manufacturer Street | FOEHRENSTR. 12 |
Manufacturer City | TUTTLINGEN, BADEN-WUERTTEMBERG 78532 |
Manufacturer Country | GM |
Manufacturer Postal Code | 78532 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HETTICH |
Generic Name | EBA 21 |
Product Code | JQC |
Date Received | 2020-01-30 |
Returned To Mfg | 2018-12-12 |
Model Number | EBA 21 |
Catalog Number | 1004 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | 4 YR |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ANDREAS HETTICH GMBH & CO. KG |
Manufacturer Address | FOEHRENSTR. 12 TUTTLINGEN, BADEN-WUERTTEMBERG 78532 GM 78532 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-30 |