MD Atlas
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Data last updated: Apr 2025
gΛt RePrint® administration tubing
3770013007025W
On Market
Class I
Regulation
EU MDR
Manufacturer
MaaT Pharma
Primary DI
03770013007026
Reference
D004-1
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Identification
Primary DI
03770013007026
Basic UDI-DI
3770013007025W
Reference
D004-1
Issuing Agency
—
ULID
RZ7VVBC0
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
MaaT Pharma
Manufacturer SRN
FR-MF-000004549
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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Market Presence
Market presence
NL
DE
FR
IT
Countries on market
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gΛt RePrint®
On Market
gΛt RePrint® collection device
On Market