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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
07640172345009 EUDAMED
Basic UDI-DI
764017234FPBJ6 EUDAMED
Direct Marketing DI
07640172345009 EUDAMED
EMDN Code
W0202059099 VARIOUS PROCESSING INSTRUMENTS FOR HYSTOLOGY / CYTOLOGY - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Denmark 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 e45fe469-dbda-4537-895c-8e60cdbea944 61 fields · synced Jun 18, 2026