MD Atlas
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Data last updated: Apr 2025
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37700238583770023858038M5
On Market
Class I
Regulation
EU MDR
Manufacturer
IMVITRO
Primary DI
03770023858038
Reference
(8012)V4.0.0
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Identification
Primary DI
03770023858038
Basic UDI-DI
37700238583770023858038M5
Reference
(8012)V4.0.0
Issuing Agency
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ULID
58PTPG3F
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
IMVITRO
Manufacturer SRN
FR-MF-000013879
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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On Market