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 2020-03-05 for DERMABOND PRINEO 22CM MSH 3.8ML ADHESIVE CLR222US manufactured by Ethicon Inc..
Report Number | 2210968-2020-01759 |
MDR Report Key | 9792840 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-05 |
Date of Report | 2020-02-07 |
Date of Event | 2020-01-01 |
Date Mfgr Received | 2020-02-07 |
Date Added to Maude | 2020-03-05 |
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 | P.O. BOX 151, ROUTE 22 WEST |
Manufacturer City | SOMERVILLE NJ 08876 |
Manufacturer Country | US |
Manufacturer Postal | 08876 |
Manufacturer Phone | 6107428552 |
Manufacturer G1 | ETHICON INC.-SAN LORENZO PR |
Manufacturer Street | ROAD 183, KM. 8.3 |
Manufacturer City | SAN LORENZO 00754 |
Manufacturer Country | * |
Manufacturer Postal Code | 00754 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DERMABOND PRINEO 22CM MSH 3.8ML ADHESIVE |
Generic Name | SURGICAL SEALANT |
Product Code | OMD |
Date Received | 2020-03-05 |
Model Number | CLR222US |
Catalog Number | CLR222US |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ETHICON INC. |
Manufacturer Address | P.O. BOX 151, ROUTE 22 WEST SOMERVILLE NJ 08876 US 08876 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-05 |