MD Atlas
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Data last updated: Apr 2025
ACL Surgery Instrumentation Case
376017704B31D3
On Market
Class I
Regulation
EU MDR
Manufacturer
TEKNIMED SAS
Primary DI
03760177049949
Reference
T067292
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Identification
Primary DI
03760177049949
Basic UDI-DI
376017704B31D3
Reference
T067292
Issuing Agency
—
ULID
R4S6FCFE
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
TEKNIMED SAS
Manufacturer SRN
FR-MF-000001224
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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