MD Atlas
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Data last updated: Apr 2025
Post Op Dech av Pied L T3
332254054KV
On Market
Class I
Regulation
EU MDR
Manufacturer
GIBAUD
Primary DI
03322541044020
Reference
8270-3
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Identification
Primary DI
03322541044020
Basic UDI-DI
332254054KV
Reference
8270-3
Issuing Agency
—
ULID
C8WNS9JN
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
GIBAUD
Manufacturer SRN
FR-MF-000014279
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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