9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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JJ Series Container System
FDA 510(k)
FDA Class 2
·General Hospital
Bernafon
FDA UDI
Bernafon AG·05711584087305·ZR1, KIT 312 NFM 85 PB R BE ZERENA 1
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776205027·LLetz Thumb Dress Forceps
OPTOMED SMARTSCOPE, MODEL M3-1 EY1
FDA 510(k)
FDA Class 2
·Ophthalmic
ECHELON 60 ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK MODEL ECR60T, ECHELON 45 ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK MODEL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
I-STAT E3+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·March 31, 2020
ISOFLEX LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 13, 2014
SINGLE EXTENSION
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·August 4, 2011