117 results · 37ms · Sources: EU EUDAMED, US FDA

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PressureWire X

FDA 510(k)
FDA Class 2 ·Cardiovascular

Comprehensive® Reverse Shoulder

FDA UDI
Biomet Orthopedics, LLC·00880304555396·

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197083645·FINOCHIETTO TC Needle holder 20 cm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197083652·FINOCHIETTO TC Needle holder 27 cm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197385626·PAR TC Needle holder, delicate 135mm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197385619·PAR TC Needle holder, delicate 12cm, ...

QUANTA DIODE LASER SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTS

FDA 510(k)
FDA Class 2 ·General Hospital

QUANTA SYSTEM S.P.A.

FDA Adverse Event
Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·December 21, 2012

COMP RVS CNTRL SCR 6.5X30MM ST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·August 30, 2018

COMP RVRS SHLDR GLNSP STD 36MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·August 29, 2018

ARCOM XL 44-36 STD HMRL BRNG

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·August 29, 2018

COMP RVRS 25MM BSPLT HA+ADPTR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·July 18, 2023

PLM A+ CANADIAN VII

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·October 15, 2014

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 20, 2013

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code MGB·July 27, 2011

COMPREHENSIVE REVERSE GLENOSPHERE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PAO·August 6, 2018

COMP RVRS 25MM BSPLT HA+ADPTR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 26, 2026

COMP NLK SCR 3.5HEX 4.75X15 ST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019

COMP LK SCR 3.5HEX 4.75X20 ST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019