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Data last updated: Apr 2025
PREPOPLUS Q50 AC
3665614-PREPO-TP-HK
On Market
Class I
Regulation
EU MDR
Manufacturer
ORTHOPLUS
Primary DI
03665614000432
Reference
PRACQ Q50
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Identification
Primary DI
03665614000432
Basic UDI-DI
3665614-PREPO-TP-HK
Reference
PRACQ Q50
Issuing Agency
—
ULID
RTK1XFPZ
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
ORTHOPLUS
Manufacturer SRN
FR-MF-000007297
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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Certificates
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DE
FR
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