MD Atlas
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Data last updated: Apr 2025
Kit patient ambu complet - Taille L-XL
3665502PROTEC3X
On Market
Class I
Regulation
EU MDR
Manufacturer
MEDISTAR
Primary DI
03665502005686
Reference
7685
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Identification
Primary DI
03665502005686
Basic UDI-DI
3665502PROTEC3X
Reference
7685
Issuing Agency
—
ULID
EKHKT929
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
MEDISTAR
Manufacturer SRN
FR-MF-000042737
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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