STEEL 88862410-69

MAUDE Adverse Event Report

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 2019-10-14 for STEEL 88862410-69 manufactured by Davis & Geck Caribe Ltd.

MAUDE Entry Details

Report Number9612501-2019-01981
MDR Report Key9187893
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-10-14
Date of Report2019-10-14
Date of Event2019-09-13
Date Mfgr Received2019-09-24
Device Manufacturer Date2019-06-28
Date Added to Maude2019-10-14
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 ContactLISA HERNANDEZ
Manufacturer Street60 MIDDLETOWN AVE.
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal06473
Manufacturer Phone2034925563
Manufacturer G1DAVIS & GECK CARIBE LTD
Manufacturer StreetZONA FRANCA DE SAN ISIDRO
Manufacturer CitySANTO DOMINGO 0101
Manufacturer CountryDO
Manufacturer Postal Code0101
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTEEL
Generic NameSUTURE, NONABSORBABLE, STEEL, MONOFILAMENT AND MULTIFILAMENT, STERILE
Product CodeGAQ
Date Received2019-10-14
Model Number88862410-69
Catalog Number88862410-69
Lot NumberD9F2768Y
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerDAVIS & GECK CARIBE LTD
Manufacturer AddressZONA FRANCA DE SAN ISIDRO SANTO DOMINGO 0101 DO 0101


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-10-14

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