MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-07-21 for UROPASS AS 11/13FR X 46 CM 5/BX 61146BX manufactured by Teleflex Medical Oem.
[80956427]
Device not yet returned.
Patient Sequence No: 1, Text Type: N, H10
[80956428]
Mhra - incident report states: ureteral access sheath was being inserted into right ureter by surgeon and it was noted that the end of catheter was split. A second ureteral sheath was used only to find that it split at the same point. Third ureteral sheath was used with same result.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3005975494-2017-00003 |
MDR Report Key | 6733905 |
Date Received | 2017-07-21 |
Date of Report | 2018-02-15 |
Date of Event | 2017-06-21 |
Date Mfgr Received | 2018-02-13 |
Date Added to Maude | 2017-07-21 |
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 | MR TERRENCE SULLIVAN |
Manufacturer Street | 136 TURNPIKE ROAD |
Manufacturer City | SOUTHBOROUGH MA 01772 |
Manufacturer Country | US |
Manufacturer Postal | 01772 |
Manufacturer Phone | 508804-273 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | UROPASS AS 11/13FR X 46 CM 5/BX |
Product Code | KNY |
Date Received | 2017-07-21 |
Returned To Mfg | 2017-07-19 |
Model Number | 61146BX |
Lot Number | 09E1600089 |
ID Number | UDI |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL OEM |
Manufacturer Address | 3750 ANNAPOLIS LANE NORTH, SUITE 160 PLYMOUTH MN 55447 US 55447 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-07-21 |