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 2019-10-28 for CRIT-LINE CLIP (CLIC) - USB CL10041001 manufactured by Concord Manufacturing.
Report Number | 2937457-2019-03254 |
MDR Report Key | 9244643 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2019-10-28 |
Date of Report | 2019-11-04 |
Date of Event | 2019-10-14 |
Date Mfgr Received | 2019-11-04 |
Device Manufacturer Date | 2017-09-14 |
Date Added to Maude | 2019-10-28 |
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 | MATTHEW AMARAL |
Manufacturer Street | 920 WINTER ST |
Manufacturer City | WALTHAM MA 02451 |
Manufacturer Country | US |
Manufacturer Postal | 02451 |
Manufacturer Phone | 7816999758 |
Manufacturer G1 | CONCORD MANUFACTURING |
Manufacturer Street | DIRECTOR, QUALITY SYSTEMS 4040 NELSON AVENUE |
Manufacturer City | CONCORD CA 94520 |
Manufacturer Country | US |
Manufacturer Postal Code | 94520 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CRIT-LINE CLIP (CLIC) - USB |
Generic Name | ACCESSORIES, BLOOD CIRCUIT, HEMODIALYSIS |
Product Code | KOC |
Date Received | 2019-10-28 |
Returned To Mfg | 2019-10-24 |
Catalog Number | CL10041001 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | MO |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CONCORD MANUFACTURING |
Manufacturer Address | DIRECTOR, QUALITY SYSTEMS 4040 NELSON AVENUE CONCORD CA 94520 US 94520 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-28 |