MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-11-13 for MICRO-INTRODUCER KITS H787065970535 manufactured by Angiodynamics, Inc.
Report Number | 1319211-2019-00103 |
MDR Report Key | 9315232 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-11-13 |
Date of Report | 2019-11-13 |
Date of Event | 2019-07-19 |
Date Mfgr Received | 2019-10-30 |
Device Manufacturer Date | 2019-07-05 |
Date Added to Maude | 2019-11-13 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | LAW RYAN |
Manufacturer Street | 10 GLENS FALLS TECHNICAL PARK |
Manufacturer City | GLENS FALLS NY 12801 |
Manufacturer Country | US |
Manufacturer Postal | 12801 |
Manufacturer Phone | 5187424488 |
Manufacturer G1 | ANGIODYNAMICS, INC |
Manufacturer Street | 603 QUEENSBURY AVENUE |
Manufacturer City | QUEENSBURY NY 12804 |
Manufacturer Country | US |
Manufacturer Postal Code | 12804 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MICRO-INTRODUCER KITS |
Generic Name | MICRO-INTRODUCER KITS |
Product Code | DQT |
Date Received | 2019-11-13 |
Returned To Mfg | 2019-11-12 |
Catalog Number | H787065970535 |
Lot Number | 5482364 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ANGIODYNAMICS, INC |
Manufacturer Address | 603 QUEENSBURY AVENUE QUEENSBURY NY 12804 US 12804 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-11-13 |