MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-25 for TRI-FUNNEL REPL GAST 24F 000724 manufactured by Bard Access Systems.
Report Number | 3006260740-2020-01058 |
MDR Report Key | 9881023 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-25 |
Date of Report | 2020-03-25 |
Date of Event | 2020-02-27 |
Date Mfgr Received | 2020-02-28 |
Date Added to Maude | 2020-03-25 |
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 | JUDITH LUDWIG |
Manufacturer Street | 1415 W. 3RD STREET |
Manufacturer City | TEMPE AZ 85281 |
Manufacturer Country | US |
Manufacturer Postal | 85281 |
Manufacturer Phone | 4803032689 |
Manufacturer G1 | PRODUCTOS PARA EL CUIDADO DE LA SALUD |
Manufacturer Street | KM. 7 CARRETERA INTERNACIONAL |
Manufacturer City | NOGALES, SONORA 85621 |
Manufacturer Country | MX |
Manufacturer Postal Code | 85621 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TRI-FUNNEL REPL GAST 24F |
Generic Name | FEEDING DEVICE |
Product Code | KNT |
Date Received | 2020-03-25 |
Model Number | 000724 |
Catalog Number | 000724 |
Lot Number | NGDP2010 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BARD ACCESS SYSTEMS |
Manufacturer Address | 605 N. 5600 W. SALT LAKE CITY UT 84116 US 84116 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-25 |