MD Atlas
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Data last updated: Apr 2025
Centura
376024624SHOULDERCPMCG
On Market
Class IIa
Regulation
EU MDR
Manufacturer
Kinetec SAS
Primary DI
03760246246903
Reference
4621003102
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Identification
Primary DI
03760246246903
Basic UDI-DI
376024624SHOULDERCPMCG
Reference
4621003102
Issuing Agency
—
ULID
5EYEDS0C
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Kinetec SAS
Manufacturer SRN
FR-MF-000000364
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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Certificates
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