28 results · 20ms · Sources: EU EUDAMED, US FDA

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COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS

FDA 510(k)
FDA Class 2 ·General Hospital

Mini-Mono®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70603161·Mini-Mono-Brackets Roth 'N' .018" 9° 1000 Brackets

neoWave LS

FDA UDI
XENIX MEDICAL LLC·00818345024113·Paddle Shaver, 16mm

Rumor

FDA UDI
Ortho Organizers, Inc.·00190707003869·Rumor .018 LR5 -22T 0A 0O

InTess Lumbar Cage

FDA UDI
Kalitec Direct LLC·B07312K0103160·Shaver, Closed, 16mm

Rumor

FDA UDI
Ortho Organizers, Inc.·00190707003876·Rumor .018 LR5 HK -22T 0A 0O

COOLTOUCH VARIA ND:YAG LASER SYSTEM; COOLTOUCH VARIA-II ND:YAG LASER SYSTEM

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

MERETEK UBT_LITE BREATH TEST FOR H. PYLORI

FDA 510(k)
FDA Class 1 ·Microbiology

XIA LP POLYAXIAL SCREW 6.5 X 40MM

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·September 20, 2011

XIA ROD DIA. 6 X 480

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·June 2, 2011

XIA BLOCKER

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·May 2, 2011

XIA SCREW 6, 5 X 40

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·May 11, 2011

XIA LP POLYAXIAL SCREW 5.5 X 45MM

FDA Adverse Event
Injury ·STRYKER SPINE-SWITZERLAND·Product code KWP·September 7, 2016

XIA POLYAXIAL SCREW 8.5 X 40MM

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code MNH·May 2, 2011

XIA BLOCKER

FDA Adverse Event
Injury ·STRYKER SPINE BORDEAUX·Product code KWP·May 11, 2011

AEQ REV II GLENOID BASEPLATE DIA 25MM

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code PHX·July 1, 2025

AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·March 13, 2025

AEQ REV GLENOID BASEPLATE 29MM

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·March 6, 2025

6MM 30CM HEMASHIELD PLAT WDV

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR·Product code MAL·April 11, 2013

UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·April 15, 2011