10,000 results · 36ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Snowden-Pencer

FDA UDI
STERIS CORPORATION·10885403458705·Snowden-Pencer MIS ERGONOMIC MODULAR JOHANN GRA...

Snowden-Pencer

FDA UDI
STERIS CORPORATION·10885403458699·Snowden-Pencer MIS ERGONOMIC MODULAR JOHANN GRA...

JSA'S REPROCESSED COMPRESSION SLEEVE DEVICES

FDA 510(k)
FDA Class 2 ·Cardiovascular

JSA REPROCESSED COMPRESSION SLEEVE DEVICES

FDA 510(k)
FDA Class 2 ·Cardiovascular

REAGENT RED BLOOD CELLS 0.8% RESOLVE PANEL C

FDA Adverse Event
Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·December 13, 2016

PANOCELL

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·January 5, 2007

1056600-2006-00530

FDA Adverse Event
Malfunction ·Product code KSZ·December 5, 2006

RESOLVE PANEL B

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 5, 2006

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·August 11, 2014

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·August 11, 2014

GALILEO

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·July 20, 2007

ID CORE XT

FDA Adverse Event
Malfunction ·PROGENIKA BIOPHARMA S.A.·Product code PEP·December 9, 2019

PANOCELL-16

FDA Adverse Event
Malfunction ·IMMUCOR·Product code KSZ·November 6, 2009

GAMMACLONE ANTI-D (MONOCLONAL BLEND)

FDA Adverse Event
Malfunction ·GAMMA BIOLOGICALS, INC.·Product code KSZ·August 4, 2006

GNS-F4 CARD

FDA Adverse Event
Malfunction ·VITEK SYSTEMS, INC.·Product code JSA·March 16, 1994

DEFENSE BLOOD STANDARD SYSTEM (DBSS)

FDA Adverse Event
Injury ·DOD/DMLSS/DBSS·Product code MMH·November 10, 2004

ECHO LUMENA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·October 31, 2024

ECHO LUMENA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·November 5, 2024

SEARCH-CYTE TCS 0.8%

FDA Adverse Event
Malfunction ·MEDION GRIFOLS DIAGNOSTICS AG,·Product code QHT·May 9, 2025

Culture Media, Antibiotic Assay

FDA classification
FDA Class 1 ·Culture Media, Antibiotic Assay