← Back to catalogue

Pathfast Sample Diluent 3

EUDAMED

Class A (EU MDR)

Ref 30003

by PHC Corporation

Identity

Trade Name
PATHFAST SAMPLE DILUENT 3 EUDAMED
Device Name
PATHFAST SAMPLE DILUENT 3 EUDAMED
Model / Reference
30003 EUDAMED

Identifiers

Primary DI / UDI-DI
04987595300035 EUDAMED
Basic UDI-DI
4987595PF03D6K EUDAMED
EMDN Code
W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Pathfast Sample Diluent 3 by Phc Corporation — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
PHC Corporation
EUDAMED SRN
JP-MF-000008516
Authorised Representative
PHC Europe B.V. NL-AR-000002692

Sources (2)

  • EUDAMED fbdb0c9e-2cc3-485e-9bd3-c84717ad4cbd 61 fields · synced Jul 10, 2026
  • EUDAMED c2e86eaf-1398-4313-91fb-ca2f71bd72bc 61 fields · synced Jul 10, 2026