26 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NON-STERILE POWDER-FREE BLUE NITRILE EXAMINATION GLOVES TESTED FOR USE WITH CHEMOTHERAPY DRUGS
FDA 510(k)
FDA Class 1
·General Hospital
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964068867·The ENDO CARRY-ON Procedure Kit contains all of...
Endeavour™ TruColor™
FDA UDI
METREX RESEARCH, LLC·00810210820196·Endeavour™ TruColor™ headlight system - North A...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450263716·
PIT AND FISSURE CHEMICAL CURING SEALANT
FDA 510(k)
FDA Class 2
·Dental
THE V-BAG
FDA 510(k)
FDA Class 2
·Cardiovascular
Biliary Plastic Stent Set
FDA UDI
Micro-Tech (Nanjing) Co., Ltd.·06932503514378·TPU,Center bend,10Fr,18cm working length with 2...
Biliary Plastic Stent Set
FDA UDI
Micro-Tech (Nanjing) Co., Ltd.·06932503514132·TPU,Side bend,10Fr,18cm working length with 220...
Biliary Plastic Stent Set/ short-wire compatible
FDA UDI
Micro-Tech (Nanjing) Co., Ltd.·06932503514880·TPU,Side bend,10Fr,18cm working length with 220...
Biliary Plastic Stent Set/ short-wire compatible
FDA UDI
Micro-Tech (Nanjing) Co., Ltd.·06932503515061·TPU,Center bend,10Fr,18cm working length with 2...
Biliary Plastic Stent Set
FDA UDI
Micro-Tech (Nanjing) Co., Ltd.·06932503515740·TPU,Straight,10Fr,18cm working length with 2200...
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 14, 2015
Widex
FDA UDI
Widex A/S·05706069720792·Widex UNIQUE U-PA BTE (Cappuccino brown S-110 )...
Widex
FDA UDI
Widex A/S·05706069726886·Widex EVOKE E-PA (Cappuccino brown S-110 ) RC coil
Widex
FDA UDI
Widex A/S·05706069722307·Widex D-PA BTE (Cappuccino brown S-110 ) RC coil
Widex
FDA UDI
Widex A/S·05706069721560·Widex UNIQUE U-FS BTE (Cappuccino brown S-110 )...
Widex
FDA UDI
Widex A/S·05706069721881·Widex D-FS BTE (Cappuccino brown S-110 ) Teleco...
Widex
FDA UDI
Widex A/S·05706069721072·Widex BEYOND B-F2 (Cappuccino brown S-110 ) Tel...
PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 3, 2013
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 10, 2011