31 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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POWDER FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE, WHITE AND GREEN COLORED. NON-STERILE, LOW DERMATITIS POTENTIAL
FDA 510(k)
FDA Class 1
·General Hospital
Chemosite
FDA UDI
Covidien LP·10884521099296·Venous Access System,120020;120039
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319719893·Tissue Forceps 6" (15cm), 2x3 teeth
AQUILION PRIME
FDA 510(k)
FDA Class 2
·Radiology
DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
STRYKER CORPORATION·04546540078636·2.1mm Cross Cut Fissure
NA
FDA UDI
STRYKER CORPORATION·07613153093794·3.2mm Cross Cut Fissure
NA
FDA UDI
STRYKER CORPORATION·04546540078629·1.6mm Cross Cut Fissure
NA
FDA UDI
STRYKER CORPORATION·04546540078612·1.2mm Cross Cut Fissure
IMPACTOR F/PFNA BLADE
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWA·December 13, 2017
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 20, 2024
Trilogy®
FDA UDI
Zimmer, Inc.·00889024361249·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024116740·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637825·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637849·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024361263·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024361256·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637818·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637832·
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·May 20, 2013