57 results · 25ms · Sources: EU EUDAMED, US FDA

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TRANSTEK BLOOD PRESSURE MONITOR MODEL TMB-986, TMB-987, TMB-995

FDA 510(k)
FDA Class 2 ·Cardiovascular

JOBST Bella Strong

FDA UDI
BSN MEDICAL, INC.·00035664012373·BELLA STRONG 20-30 MM HG GAUNTLET SIZE 5 NATURA...

Tasso+ Convenience Kit

FDA UDI
Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...

Luxe™ 2.5 Semi-custom loupe

FDA UDI
METREX RESEARCH, LLC·00850036373568·Semi-custom loupe with Luxe™ 2.5 plano oculars,...

Best Medical International

FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365119200·

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383502146·Gutta Percha Points is used to root canal filin...

BEL-CAT

FDA 510(k)
FDA Class 2 ·Radiology

POSITRACE DUAL MODE PET/CT ONCOLOGY SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

AS VEGA PS TIBIAL PLATEAU CEMENTED T3

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 4, 2018

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 3, 2013

AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

FDA Adverse Event
Malfunction ·UNKNOWN·Product code FNL·September 19, 2014

INTERSTIM

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·May 11, 2011

AS COLUMBUS REV F FEMUR CEMENTED F5L

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

AS VEGA PS TIBIAL PLATEAU CEMENTED T3+

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

AS VEGA PS TIBIAL PLATEAU CEMENTED T2

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

AS COLUMBUS REV F TIB.OFFSET CEMENT.T5

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

LGC TIBIAL FIT TRAY CEM SZ 3.5F / 3.5T

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

UNK STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 8, 2025

UNKNOWN HEAD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 26, 2025

UNK TRILOGY SHELL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 24, 2025