30 results
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24ms
·
Sources: EU EUDAMED, US FDA
NT SWIFT; TI\TEC; GATES GLIDDEN DRILLS; DENTAL POWER ENDODONTIC HAND FILES
FDA 510(k)
FDA Class 1
·Dental
artegral life HD
FDA UDI
Merz Dental GmbH·D7092004031·artegral life HighDefinition posterior lower -M...
Erythrocyte Fragility (osmotic)
FDA UDI
BIOANALYTIC GmbH, biomed. Analysentechnik·04061609000309·
Mendaera Probe and Robot Drape Kit
FDA UDI
Mendaera, Inc.·00850062065086·
Generic Buccal Tubes
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746125843·TUBE MAX MOLAR 022/045 INCONEL TQ=0 R=0 4.5MM R...
EryFragility-TIC (osmotic Erythrocyte Fragility)
FDA UDI
BIOANALYTIC GmbH, biomed. Analysentechnik·04061609000316·
Inspire
FDA UDI
Inspire Medical Systems, Inc.·00855728005109·The Model 2740 physician programmer is designed...
Xcel
FDA UDI
STRYKER CORPORATION·07613154083299·3MM X 24MM XCEL DRILL
AQUANET, MODEL EC 2000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
URANUS, COMFORTOUCH LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEYER-SCHULTE SALINE-FILLED MAMMARY PROSTHESIS, 275 CC
FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FWM·November 15, 1994
AVENIR MLLER, STEM, STANDARD, UNCEMENTED, HA, 4, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·August 13, 2021
GEMSTAR PAIN MGE SNG
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·August 30, 2013
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·November 20, 2010
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·March 12, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2011
PRECISION XTRA/OPTIUM
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·February 26, 2008
VERSA-DIAL 46X24X47 HUM HEAD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·April 24, 2013
PC HYBRID GLENOID POST- POLY
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013
SM HYBRID GLENOID BASE 4MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013