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

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VENUS Bracket, ROSE Bracket

FDA 510(k)
FDA Class 2 ·Dental

Zodiac

FDA UDI
ALPHATEC SPINE, INC.·00844856002562·PRE CONTOURED CP ROD 5.5 x 10cm NON-BROACHED

Ophthlamic Speculum

FDA UDI
KATENA PRODUCTS, INC.·10841668112424·DISPOSABLE BARRAQUER SPECULUM BOX OF 10

Accufit

FDA UDI
Ortho Organizers, Inc.·00190707183936·Accufit Molar Bands Lower Right First Molar 41

OsteoMed

FDA UDI
OSTEOMED LLC·00845694019620·1.0mm Drill, J-Latch

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383556316·"An absorbent paper points is an endodontic pap...

PHORESOR MODEL PM2000

FDA 510(k)
FDA Class 2 ·Physical Medicine

AQUASIL ULTRA XLV SMART WETTING IMPRESSION MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

R3 48MM ID US COCR LNR MM60

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·July 5, 2018

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code LFR·February 12, 2015

HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC.·Product code DSQ·July 31, 2018

I-STAT PT/INRCARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code GJS·October 14, 2014

I-STAT TROPONIN (CTNI) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code MMI·August 20, 2014

HEARTWARE VENTRICULAR ASSIST SYSTEM- CONTROLLER 1.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC.·Product code DSQ·June 13, 2018

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·May 5, 2015

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code LFR·February 12, 2015

HEARTWARE VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Malfunction ·HEARTWARE, INC·Product code DSQ·March 23, 2017

HEARTWARE® VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC·Product code DSQ·September 15, 2017

I-STAT TROPONIN (CTNI) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code MMI·June 24, 2014

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code LFR·July 9, 2015