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Xmark Fix - 250ml

EUDAMED

Class A (EU MDR)

Ref RCB-0100-00A

by CellPath Ltd

Identity

Trade Name
XMARK FIX - 250ML EUDAMED
Device Name
XMark EUDAMED
Model / Reference
RCB-0100-00A EUDAMED

Identifiers

Primary DI / UDI-DI
05056256114225 EUDAMED
Basic UDI-DI
05056256RCA00144 EUDAMED
EMDN Code
W01030708 STAIN SOLUTIONS (HISTOLOGY/CYTOLOGY) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

Xmark Fix - 250ml by CellPath Ltd — 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
CellPath Ltd
EUDAMED SRN
GB-MF-000022744
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 859ee435-ef1e-4655-85c6-042bedd63f4d 61 fields · synced Jul 10, 2026