MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,08 report with the FDA on 2015-03-26 for URINARY CATHETER 02016559 manufactured by Unomedical S.r.o..
[5617535]
It was reported that upon receipt, the urinary catheter appeared to have been "folded". No pt involvement was reported.
Patient Sequence No: 1, Text Type: D, B5
[13097064]
Based on the available info, this event is deemed a reportable malfunction. There were no reports of the pt being harmed as a result of this malfunction. Additional pt/event details have been requested. Should additional info become available, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3005778470-2015-00005 |
MDR Report Key | 4641722 |
Report Source | 01,08 |
Date Received | 2015-03-26 |
Date of Report | 2015-02-20 |
Date Mfgr Received | 2015-02-20 |
Date Added to Maude | 2015-05-08 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | MATTHEW WALENCIAK, INTE ASSO DIR |
Manufacturer Street | 211 AMERICAN AVE. |
Manufacturer City | GREENSBORO NC 27409 |
Manufacturer Country | US |
Manufacturer Postal | 27409 |
Manufacturer Phone | 9083779293 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | URINARY CATHETER |
Generic Name | CONNECTOR, CATHETER |
Product Code | GCD |
Date Received | 2015-03-26 |
Model Number | 02016559 |
Lot Number | 169016 |
Operator | OTHER |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | UNOMEDICAL S.R.O. |
Manufacturer Address | PRIEMYSELNY PARK 3 MICHALOVCE 07101 LO 07101 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-03-26 |