10,000 results · 32ms · Sources: EU EUDAMED, US FDA

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Anti-Jka

FDA UDI
IMMUCOR, INC.·10888234000815·This reagent is used for the detection of the J...

Anti-Jka (JK1)

FDA UDI
DIAGAST·23661562105346·Blood Grouping Reagent, Anti-Jka (Human/Murine ...

ALBAclone Anti-Jka (Monoclonal)

FDA UDI
ALBA BIOSCIENCE LIMITED·05060242472480·This Anti-Jka reagent is for the in vitro detec...

ALBAclone Anti-Jka (Monoclonal)

FDA UDI
ALBA BIOSCIENCE LIMITED·05060242471704·This Anti-Jka reagent is for the in vitro detec...

ORTHOTM Sera Anti-Jka

FDA UDI
ALBA BIOSCIENCE LIMITED·10758750013029·The Anti-Jka reagent (Anti-JK1) is for the qual...

Anti-Jka (Human/Murine Monoclonal)

FDA UDI
American National Red Cross·00858400005190·Blood Grouping Reagent

Seraclone® Anti-Jka (JK1)

FDA UDI
Bio-Rad Medical Diagnostics GmbH·07611969951758·Blood Grouping Reagent Anti-Jka (JK1); Seraclon...

Anti-Jka (Monoclonal) Gamma-clone

FDA UDI
IMMUCOR, INC.·10888234002185·This reagent is used for the detection of the J...

Anti-Jka Coombs-reactive, polyclonal, human

Device
EU IVDD · Eu Ivd Annex 2 List B ·ANTITOXIN GmbH·On the market

Anti-Jka monoclonal, human IgM clone: MS-15

Device
EU IVDD · Eu Ivd Annex 2 List B ·ANTITOXIN GmbH·On the market

Anti-Jka for card method, Coombs-reactive, polyclonal, human

Device
EU IVDD · Eu Ivd Annex 2 List B ·ANTITOXIN GmbH·On the market

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·March 21, 2012

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·June 3, 2014

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·June 7, 2012

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·July 30, 2014

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·October 29, 2014

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·July 2, 2012

ANTI-JKA

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·June 30, 2015

GALILEO ECHO

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·May 13, 2015

ID CORE XT

FDA Adverse Event
Malfunction ·PROGENIKA BIOPHARMA S.A.·Product code PEP·July 3, 2020