MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,s report with the FDA on 2019-07-24 for VENOVO VENOUS STENT SYSTEM VENEM14140 manufactured by Angiomed Gmbh & Co. Medizintechnik Kg.
Report Number | 9681442-2019-00137 |
MDR Report Key | 8822732 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,S |
Date Received | 2019-07-24 |
Date of Report | 2019-07-24 |
Date of Event | 2019-06-26 |
Date Mfgr Received | 2019-06-27 |
Device Manufacturer Date | 2016-02-05 |
Date Added to Maude | 2019-07-24 |
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 | JUDITH LUDWIG |
Manufacturer Street | 1625 W 3RD ST. |
Manufacturer City | TEMPE AZ 85281 |
Manufacturer Country | US |
Manufacturer Postal | 85281 |
Manufacturer Phone | 4803032689 |
Manufacturer G1 | ANGIOMED GMBH & CO. MEDIZINTECHNIK KG |
Manufacturer Street | WACHHAUSSTRASSE 6 |
Manufacturer City | KARLSRUHE 76227 |
Manufacturer Country | GM |
Manufacturer Postal Code | 76227 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VENOVO VENOUS STENT SYSTEM |
Generic Name | VENOUS STENT SYSTEM |
Product Code | QAN |
Date Received | 2019-07-24 |
Catalog Number | VENEM14140 |
Lot Number | ANAY0263 |
Device Expiration Date | 2018-01-27 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ANGIOMED GMBH & CO. MEDIZINTECHNIK KG |
Manufacturer Address | WACHHAUSSTRASSE 6 KARLSRUHE 76227 GM 76227 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2019-07-24 |