MD Atlas
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Data last updated: Apr 2025
Needle #1
B-03662674000075
On Market
Class IIa
Regulation
EU MDR
Manufacturer
SpineGuard.S.A
Primary DI
03662674000075
Reference
P2ND1001
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Identification
Primary DI
03662674000075
Basic UDI-DI
B-03662674000075
Reference
P2ND1001
Issuing Agency
—
ULID
CSPXGHEF
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
SpineGuard.S.A
Manufacturer SRN
FR-MF-000004720
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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