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 2020-02-20 for HEMOSPRAY ENDOSCOPIC HEMOSTAT HEMO-7-EU manufactured by Cook Endoscopy.
Report Number | 1037905-2020-00090 |
MDR Report Key | 9734781 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-02-20 |
Date of Report | 2020-01-28 |
Date of Event | 2020-01-28 |
Date Mfgr Received | 2020-01-28 |
Device Manufacturer Date | 2019-04-23 |
Date Added to Maude | 2020-02-20 |
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 | MS. SCOTTIE FARIOLE |
Manufacturer Street | 4900 BETHANIA STATION RD |
Manufacturer City | WINSTON-SALEM NC 27105 |
Manufacturer Country | US |
Manufacturer Postal | 27105 |
Manufacturer Phone | 3367440157 |
Manufacturer G1 | COOK ENDOSCOPY |
Manufacturer Street | 4900 BETHANIA STATION RD |
Manufacturer City | WINSTON-SALEM NC 27105 |
Manufacturer Country | US |
Manufacturer Postal Code | 27105 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HEMOSPRAY ENDOSCOPIC HEMOSTAT |
Product Code | QAU |
Date Received | 2020-02-20 |
Returned To Mfg | 2020-02-24 |
Catalog Number | HEMO-7-EU |
Lot Number | W4204867 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOK ENDOSCOPY |
Manufacturer Address | 4900 BETHANIA STATION RD WINSTON-SALEM NC 27105 US 27105 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-20 |