25 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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OXYRASE, INC.
FDA registration
OXYRASE, INC.·3 products·🇺🇸 United States
OxyPRAS Anaselect Blood Agar plate
FDA UDI
Oxyrase, Inc.·00850056467032·Culture Media, Selective and Non-Differential
PEA OxyPlate
FDA UDI
Oxyrase, Inc.·00850056467124·Culture Media, Selective and Non-Differential
Schaedler Blood Agar OxyPlate
FDA UDI
Oxyrase, Inc.·00850056467063·Culture Media, Enriched
OxyPRAS Plus Bile Esculin plate
FDA UDI
Oxyrase, Inc.·00850056467056·Culture Media, Selective and Non-Differential
OxyPRAS Plus 3-pack: Brucella, PEA and BBE/KVL Bi-Plate
FDA UDI
Oxyrase, Inc.·00850056467094·Culture Media, Selective and Non-Differential
OxyPRAS Plus StrictAna Blood Agar Plate with Gentamycin
FDA UDI
Oxyrase, Inc.·00850056467131·Culture Media, Selective and Non-Differential
Modified Columbia Agar plate
FDA UDI
Oxyrase, Inc.·00850056467087·Culture Media, Selective and Non-Differential
OxyPRAS Plus KVL plate
FDA UDI
Oxyrase, Inc.·00850056467049·Culture Media, Selective and Non-Differential
OxyPRAS Plus 2-pack, Brucella and BBE/KVL Bi-Plate
FDA UDI
Oxyrase, Inc.·00850056467117·Culture Media, Selective and Non-Differential
OxyPRAS Plus Brucella Agar plate
FDA UDI
Oxyrase, Inc.·00850056467001·Cultured Media, Non-Selective and Non-Differential
OxyPRAS Plus 3-pack, Brucella, PEA, and KVL
FDA UDI
Oxyrase, Inc.·00850056467100·Culture Media, Selective and Non-Differential
OxyPRAS Plus BBE/KVL Bi-Plate
FDA UDI
Oxyrase, Inc.·00850056467025·Culture Media, Selective and Non-Differential
OxyPRAS Plus PEA Plate
FDA UDI
Oxyrase, Inc.·00850056467018·Culture Media, Selective and Non-Differential
KVL OxyPlate
FDA UDI
Oxyrase, Inc.·00850056467070·Culture Media, Selective and Non-Differential
REMEL
FDA Adverse Event
Malfunction
·REMEL·Product code JSM·June 26, 2002
BBL
FDA Adverse Event
Malfunction
·BBL·Product code JSM·June 26, 2002
OXYRASE
FDA Adverse Event
Malfunction
·OXYRASE, INC.·Product code JSM·June 26, 2002
BBL
FDA Adverse Event
Malfunction
·BBL·Product code JSM·June 26, 2002
OXYRASE
FDA Adverse Event
Malfunction
·OXYRASE, INC.·Product code JSM·June 26, 2002