TRACER METRO DIRECT WIRE GUIDE METII-21-480

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-02-24 for TRACER METRO DIRECT WIRE GUIDE METII-21-480 manufactured by Cook Endoscopy.

MAUDE Entry Details

Report Number1037905-2020-00101
MDR Report Key9746911
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-02-24
Date of Report2020-01-28
Date of Event2020-01-28
Date Mfgr Received2020-01-28
Date Added to Maude2020-02-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. SCOTTIE FARIOLE
Manufacturer Street4900 BETHANIA STATION RD
Manufacturer CityWINSTON-SALEM NC 27105
Manufacturer CountryUS
Manufacturer Postal27105
Manufacturer Phone3367440157
Manufacturer G1COOK ENDOSCOPY
Manufacturer Street4900 BETHANIA STATION RD
Manufacturer CityWINSTON-SALEM NC 27105
Manufacturer CountryUS
Manufacturer Postal Code27105
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRACER METRO DIRECT WIRE GUIDE
Generic NameOCY ENDOSCOPIC GUIDEWIRE, GASTROENTEROLOGY-UROLOGY
Product CodeOCY
Date Received2020-02-24
Catalog NumberMETII-21-480
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOK ENDOSCOPY
Manufacturer Address4900 BETHANIA STATION RD WINSTON-SALEM NC 27105 US 27105


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.