46 results · 24ms · Sources: EU EUDAMED, US FDA

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Keeogo Dermoskeleton System

FDA 510(k)
FDA Class 2 ·Physical Medicine

EarQ

FDA UDI
Oticon A/S·05707131350411·G50 S, BTE PP 13 2.4G 105 C044 EARQ

FAC-4 - Duke Power Cabinet

FDA UDI
Certified Safety Manufacturing, Inc.·00766588015293·FAC-4 - Duke Power Cabinet

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383512244·"An absorbent paper points is an endodontic pap...

DERMASSIST FLUID RESISTANT SURGICAL MASK (ORANGE) AND PROCEDURE MASK WITH TIE-ON AND WITH EARLOOPS

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

RENU MULTIPLUS MULTI-PURPOSE SOLUTION

FDA 510(k)
FDA Class 2 ·Ophthalmic

UNKNOWN STEM

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code JDG·February 13, 2017

UNKNOWN HEAD

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·February 14, 2017

UNKNOWN LINER

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·February 14, 2017

ACCU-CHEK ® COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 17, 2015

UNKNOWN TRILOGY CUP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 14, 2017

UNKNOWN LINER

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 14, 2017

UNKNOWN HEAD

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 14, 2017

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 14, 2017

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 14, 2017

UNKNOWN LINER

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 13, 2017

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·February 13, 2017

UNKNOWN TRILOGY GENERIC HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LZO·February 13, 2017

UNKNOWN HEAD

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·February 13, 2017

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·February 14, 2017