3,163 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNERGY PRECISION BIPOLAR COAGULATOR
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code GEI·June 18, 2014
SYNERGY PRECISION BIPOLAR COAGULATOR
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GEI·February 17, 2015
CMC-V GENERATOR ENGLISH
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC·Product code GEI·January 3, 2014
GAMMA CORE DEVICE
FDA Adverse Event
Injury
·UNK·Product code QAK·November 27, 2018
Non-Invasive Vagus Nerve Stimulator For Migraine Headache
FDA classification
FDA Class 2
·Non-Invasive Vagus Nerve Stimulator For Migraine Headache
MAK-SYSTEM CORP.
FDA registration
MAK-SYSTEM CORP.·1 product·🇺🇸 United States
AMII AMERICA KIT
FDA UDI
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)·08809986680235·
BAK KOHLER Medical KG
FDA registration
BAK KOHLER Medical KG·16 products·🇩🇪 Germany
MAK-SYSTEM Group Ltd.
FDA registration
MAK-SYSTEM Group Ltd.·1 product·🇬🇧 United Kingdom
JAK DIVERSIFIED II, INC.
FDA registration
JAK DIVERSIFIED II, INC.·3 products·🇺🇸 United States
Endo Access
FDA UDI
TULSA DENTAL PRODUCTS LLC·D716EAK1·Endo Access Kit - Holder & Ins
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333192·
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333222·
BAK®
FDA UDI
BIOMET SPINE LLC·00887868259975·
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333352·
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333154·
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333130·
BAK®
FDA UDI
BIOMET SPINE LLC·00887868259968·
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333185·
BAK®
FDA UDI
BIOMET SPINE LLC·00887868259982·