MD Atlas
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Data last updated: Apr 2025
CRYOSTAB® GO
37014598EPAIMM001ST9K
On Market
Class I
Regulation
EU MDR
Manufacturer
GROUPE SOBER SAS
Primary DI
03760035448747
Reference
CRYOSTAB® GO
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Identification
Primary DI
03760035448747
Basic UDI-DI
37014598EPAIMM001ST9K
Reference
CRYOSTAB® GO
Issuing Agency
—
ULID
GP888VZ9
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
GROUPE SOBER SAS
Manufacturer SRN
FR-MF-000017818
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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