MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-10-01 for 4FR X 20CM SINGLE LUMEN CT MIDLINE BASIC TRAY VYML4S1001 manufactured by Vygon Usa.
Report Number | 2245270-2019-00062 |
MDR Report Key | 9139823 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-10-01 |
Date of Report | 2019-11-08 |
Date of Event | 2019-09-22 |
Date Mfgr Received | 2019-09-23 |
Date Added to Maude | 2019-10-01 |
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 | CLAIRE PADDOCK |
Manufacturer Street | 2750 MORRIS ROAD |
Manufacturer City | LANSDALE PA 19446 |
Manufacturer Country | US |
Manufacturer Postal | 19446 |
Manufacturer Phone | 8004735414 |
Manufacturer G1 | VYGON MFG |
Manufacturer Street | 87 VENTURE DRIVE |
Manufacturer City | DOVER NH 03820 |
Manufacturer Country | US |
Manufacturer Postal Code | 03820 |
Single Use | 3 |
Remedial Action | RC |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 4FR X 20CM SINGLE LUMEN CT MIDLINE BASIC TRAY |
Generic Name | MIDLINE CATHETER |
Product Code | PND |
Date Received | 2019-10-01 |
Model Number | VYML4S1001 |
Catalog Number | VYML4S1001 |
Lot Number | 19G020D |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | VYGON USA |
Manufacturer Address | 2750 MORRIS ROAD LANSDALE PA 19446 US 19446 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-01 |