MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-03 for PROTECTION SLEEVE FOR FNS INSERTION INSTRUMENTS 03.168.013 manufactured by Oberdorf Synthes Produktions Gmbh.
Report Number | 8030965-2019-67940 |
MDR Report Key | 8958050 |
Date Received | 2019-09-03 |
Date of Report | 2019-08-05 |
Date of Event | 2019-07-30 |
Date Mfgr Received | 2019-10-10 |
Device Manufacturer Date | 2018-07-16 |
Date Added to Maude | 2019-09-03 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KARA DITTY-BOVARD |
Manufacturer Street | EIMATTSTRASSE 3 |
Manufacturer City | OBERDORF 4436 |
Manufacturer Country | SZ |
Manufacturer Postal | 4436 |
Manufacturer Phone | 6103142063 |
Manufacturer G1 | SYNTHES SELZACH |
Manufacturer Street | BOHACKERWEG 5 |
Manufacturer City | SELZACH 2545 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 2545 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PROTECTION SLEEVE FOR FNS INSERTION INSTRUMENTS |
Generic Name | CANNULA,SURGICAL,GENERAL & PLASTIC SURGERY |
Product Code | GEA |
Date Received | 2019-09-03 |
Returned To Mfg | 2019-09-10 |
Catalog Number | 03.168.013 |
Lot Number | 180067-104 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
Manufacturer Address | EIMATTSTRASSE 3 OBERDORF 4436 SZ 4436 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-03 |