39 results · 22ms · Sources: EU EUDAMED, US FDA

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RIDA GENE Norovirus GI/GII

FDA 510(k)
FDA Class 2 ·Microbiology

SR MCP

FDA UDI
Stryker GmbH·00886385020815·S.R. MCP PHALANGEAL TRIAL, SIZE SM

Life Instruments

FDA UDI
Life Instrument Corporation·M930717151110·Thoracic Ring Curette #1 Angled

Life Instruments

FDA UDI
Life Instrument Corporation·M930717151100·Thoracic Ring Curette #1

PLEXUS HERPESELECT 1 AND 2 IGG (WITH PLEXUS TM SOFTWARE), MODEL MP0900G

FDA 510(k)
FDA Class 2 ·Microbiology

MACLIN POWER INTRAVASCULAR ADMINISTRATION SET

FDA 510(k)
FDA Class 2 ·General Hospital

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118236·SA Cervical Cage, 17.5mm x 15mm x 11mm, 2° Lord...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120437·17.5mm x 15mm x 11mm 2° Lordotic Trial/Broach w...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120505·17.5mm x 15mm x 11mm 7° Lordotic Trial/Broach w...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133543·Assembly, T3 SA Cervical Cage, 17.5mm x 15mm x ...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118373·SA Cervical Cage, 17.5mm x 15mm x 11mm, 7° Lord...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133819·NSA Cervical Cage, 17.5mm x 15mm x 11mm, 7° Lor...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133420·Assembly, T3 SA Cervical Cage, 17.5mm x 15mm x ...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523133741·NSA Cervical Cage, 17.5mm x 15mm x 11mm, 2° Lor...

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

FDA Adverse Event
Malfunction ·CAREFUSION, INC·Product code KNW·March 12, 2026

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·March 13, 2019

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

ARGON BEAM COAGULATOR

FDA Adverse Event
Malfunction ·CONMED·Product code GEI·July 15, 2011