MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-25 for CLEARGUARD HD ANTIMICROBIAL BARRIER CAP CGHD CGHD-100 manufactured by Pursuit Vascular, Inc..
Report Number | 3011277191-2020-00001 |
MDR Report Key | 9880910 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-03-25 |
Date of Report | 2020-03-25 |
Date of Event | 2020-01-31 |
Date Mfgr Received | 2020-02-25 |
Device Manufacturer Date | 2019-11-21 |
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 | MR. JAYSON BABLER |
Manufacturer Street | 6901 EAST FISH LAKE ROAD SUITE 166 |
Manufacturer City | MAPLE GROVE, MN |
Manufacturer Country | US |
Manufacturer Phone | 3344284 |
Manufacturer G1 | PURSUIT VASCULAR, INC. |
Manufacturer Street | 6901 EAST FISH LAKE ROAD SUITE 166 |
Manufacturer City | MAPLE GROVE, MN |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLEARGUARD HD ANTIMICROBIAL BARRIER CAP |
Generic Name | CLEARGUARD HD ANTIMICROBIAL BARRIER CAP |
Product Code | PEH |
Date Received | 2020-03-25 |
Model Number | CGHD |
Catalog Number | CGHD-100 |
Lot Number | 6118 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PURSUIT VASCULAR, INC. |
Manufacturer Address | 6901 EAST FISH LAKE ROAD SUITE 166 MAPLE GROVE, MN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-25 |