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Procise Stool Collection Kit

EUDAMED

Class A (EU MDR)

Ref 4913

by ProciseDx Inc.

Identity

Trade Name
Procise Stool Collection Kit EUDAMED
Device Name
Procise Stool Collection Kit EUDAMED
Model / Reference
4913 EUDAMED

Identifiers

Primary DI / UDI-DI
08100322949130 EUDAMED
Basic UDI-DI
081003229PDXE491222VJ EUDAMED
Direct Marketing DI
08100322949130 EUDAMED
EMDN Code
W05019001 FAECES COLLECTION DEVICES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Procise Stool Collection Kit by ProciseDx Inc. — 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
ProciseDx Inc.
EUDAMED SRN
US-MF-000040747
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 58d0680d-b6dc-4c44-9e99-5b1976d8e1fa 61 fields · synced Jun 19, 2026