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FlexPath Blox

EUDAMED

Class A (EU MDR)

Ref FPB

by Inpeco SA

Identity

Trade Name
FlexPath Blox EUDAMED
Device Name
FlexPath EUDAMED
Model / Reference
FPB EUDAMED

Identifiers

Primary DI / UDI-DI
07640172345016 EUDAMED
Basic UDI-DI
764017234FPBJ6 EUDAMED
Direct Marketing DI
07640172345016 EUDAMED
EMDN Code
W0202059004 TISSUE EMBEDDING PROCESSORS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Norway EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

FlexPath Blox by Inpeco SA — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Inpeco SA
EUDAMED SRN
CH-MF-000017833
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 96ac50d5-dc9f-4072-b659-6cd4ddab735b 61 fields · synced Jun 19, 2026