2,758 results · 25ms · Sources: EU EUDAMED, US FDA

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HLE - Creamy - 4oz

FDA UDI
CC Wellness LLC·00796494003404·Hybrid Personal Lubricant

HLE-1000 HIGH/LOW TREATMENT TABLE

FDA 510(k)
FDA Class 1 ·Physical Medicine

1.5T Endorectal Coil

FDA UDI
RAPID Biomedical GmbH·04260487680232·1.5T Endorectal Coil (P-Port)

3.0T Endorectal Coil

FDA UDI
RAPID Biomedical GmbH·04260487680249·3.0T Endorectal Coil

1.5T Endorectal Coil

FDA UDI
RAPID Biomedical GmbH·04260487680416·1.5T Endorectal Coil (A-Port)

UNK_ULTRACISION HARMONIC FOCUS

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 20, 2022

DEPUY PINNACLE 100 ACETABULAR CUP SZ 56 MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·July 24, 2013

ACL DISPOSABLE PACK BONE-TENDON-BONE

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code KDD·February 10, 2016

TAPERLOC MICRO LAT FMRL 11MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 10, 2018

EPOLY 36MM RINGLC LNR HW SZ24

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 10, 2018

36MM COCR MOD HD -6MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 10, 2018

28MM MOD HD STD NECK TP1 TAPER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 24, 2018

UNKNOWN LINER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 24, 2018

MLRY-HD POR FMRL 9X150MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·September 13, 2018

ARCOM 28MM RNGLOC LNR HWALL 22

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 15, 2018

PAT RMR BLD W/PILOT HLE

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HTO·July 1, 2019

E1 RINGLOC ACETABULAR LINER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 8, 2018

28MM MOD HD STD NECK TP1 TAPER

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·September 13, 2018

MODULAR HEAD COMPONENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 8, 2018

UNKNOWN HEAD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 15, 2018