MD Atlas
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Data last updated: Apr 2025
SENTRY MD98000120
376033037ADAPTATION1DD
On Market
Class I
Regulation
EU MDR
Manufacturer
MEDIDEV - SENTECH FRANCE
Primary DI
03760330371085
Reference
MD98000120
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Identification
Primary DI
03760330371085
Basic UDI-DI
376033037ADAPTATION1DD
Reference
MD98000120
Issuing Agency
—
ULID
GT8WCSNK
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
MEDIDEV - SENTECH FRANCE
Manufacturer SRN
FR-MF-000008021
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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