39 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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