MD Atlas
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Data last updated: Apr 2025
ManyFlow D 2 Vial
B-13700550400353
On Market
Class IIa
Regulation
EU MDR
Manufacturer
MEDEX
Primary DI
13700550400353
Reference
FSDMU240
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Identification
Primary DI
13700550400353
Basic UDI-DI
B-13700550400353
Reference
FSDMU240
Issuing Agency
—
ULID
1XWWET8M
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
MEDEX
Manufacturer SRN
FR-MF-000000414
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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