MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-30 for HUDSON ET TUBE HOLDER, STANDARD, W/BITE BLOCK 81802 manufactured by Teleflex Medical Sdn. Bhd..
Report Number | 8040412-2020-00092 |
MDR Report Key | 9897760 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2020-03-30 |
Date of Report | 2020-03-12 |
Date of Event | 2020-03-11 |
Date Mfgr Received | 2020-03-12 |
Date Added to Maude | 2020-03-30 |
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 | VICTORIA SANDLIN |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer G1 | TELEFLEX MEDICAL SDN. BHD. |
Manufacturer Street | LOT NO : PT2577 JALEN PERUSAHAAN 4 KAMUNTING INDUSTRIAL ESTATE |
Manufacturer City | PERAK, WEST MALAYSIA 34600 |
Manufacturer Country | MY |
Manufacturer Postal Code | 34600 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUDSON ET TUBE HOLDER, STANDARD, W/BITE BLOCK |
Generic Name | TRACHEAL TUBE FIXATION DEVICE |
Product Code | CBH |
Date Received | 2020-03-30 |
Catalog Number | 81802 |
Lot Number | 35076 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL SDN. BHD. |
Manufacturer Address | PERAK, WEST MALAYSIA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |