10,000 results · 40ms · 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.

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749060980·CERAMO punch with ejector flatfoot, 90° upw., 2...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064919·CERAMO TRADITION X punch calib., 40° upw., 4.0x...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064940·CERAMO TRADITION X punch calib., 40° upw., 5.0x...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064780·CERAMO punch with ejector APART,cali 40° upw.2....

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064865·CERAMO punch with ejector, calibrated, 40° upw....

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064803·CERAMO punch with ejector 40° upw., 2.0 x 200 mm

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749001792·CERAMO TRADITION X punch 40° upw., 2.0 x 200 mm

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064933·CERAMO punch with ejector, calibrated, 40° upw....

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749064872·CERAMO TRADITION X punch calib., 40° upw., 3.0x...

NNI

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·December 14, 2015

UNKNOWN ZMR CONE BODY

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LZO·May 8, 2017

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·May 8, 2017

PALMAZ XL STENT PER 40MM UNMOUNTED

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code FGE·May 29, 2014

TWO-PEDAL FOOTSWITCH; VIO®3 REMODE; BRACKET; MIDDLE PIECE

FDA Adverse Event
Malfunction ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·November 12, 2025

CNS-6201A

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·September 29, 2020

CNS-6801A

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·November 7, 2019

CNS-6201A

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·November 22, 2019

CSF-SNAP SHUNT VENTRICULAR CATHETER KIT

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·September 10, 2020

CNS-6801A

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·November 30, 2021

SURESCAN

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·December 18, 2019