MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-03-19 for 3.5MM POPLOK SUTURE ANCHOR CKP-3500 manufactured by Conmed Corporation.
Report Number | 1017294-2020-00137 |
MDR Report Key | 9856356 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2020-03-19 |
Date of Report | 2020-03-19 |
Date of Event | 2020-02-11 |
Date Mfgr Received | 2020-02-25 |
Date Added to Maude | 2020-03-19 |
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 | MS TRACEY WEISELBENTON |
Manufacturer Street | 11311 CONCEPT BLVD |
Manufacturer City | LARGO, FL |
Manufacturer Country | US |
Manufacturer Phone | 3995557 |
Manufacturer G1 | CONMED CORPORATION |
Manufacturer Street | 11311 CONCEPT BLVD |
Manufacturer City | LARGO, FL |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 3.5MM POPLOK SUTURE ANCHOR |
Generic Name | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Product Code | MBI |
Date Received | 2020-03-19 |
Catalog Number | CKP-3500 |
Lot Number | 1047419 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CONMED CORPORATION |
Manufacturer Address | 11311 CONCEPT BLVD LARGO, FL US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-19 |