51 results · 22ms · Sources: EU EUDAMED, US FDA

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DANEK IRRIGATING BURR (DIB) SET

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690127321·Apex Revision Knee System-Revision Femur Instru...

RINGLOC TRI-POLAR LINER SIZE 27

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·August 21, 2018

ENDO II TAPER INSERT +6MM T1

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 21, 2018

ENDO II MOD ENDO HEAD SZ 44

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 21, 2018

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690194934·Apex Revision Knee System-Revision Femur Instru...

Portex

FDA UDI
ICU MEDICAL, INC.·15019315060403·

DETERMINATION OF ANTITHROMBIN III, 885

FDA 510(k)
FDA Class 2 ·Hematology

DynoSense Vital Sign Measuring System

FDA 510(k)
FDA Class 2 ·Cardiovascular

VerSys Heritage® Hip Prosthesis

FDA UDI
Zimmer, Inc.·00889024140356·

SUPRAMID BLACK 5/0 (1) 45CM DS16

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·January 17, 2019

COBE SPECTRA APHERESIS SYSTEM TPE SET

FDA Adverse Event
Injury ·CARIDIANBCT·Product code LKN·October 28, 2010

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 7, 2014

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012

SUPRAMID WHITE 2/0 (3) 100M

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·November 4, 2019

SUPRAMID BLACK 4/0 (1.5) 45CM HS15

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·July 31, 2019

DAFILON BLUE 2/0 (3) 75CM DS24 (M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·July 1, 2019

DAFILON BLUE 4/0 (1.5) 45CM DS16 (M)

FDA Adverse Event
Injury ·B.BRAUN SURGICAL SA·Product code GAR·October 15, 2019

DAFILON BLUE 2/0 (3) 75CM DS30

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·October 4, 2019

SUPRAMID BLACK 2/0 (3) 5X45CM

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·August 20, 2020