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Biopad Biopsy Pad - Black

EUDAMED

Class A (EU MDR)

Ref EBA-0101-03AModel BIOPAD BIOPSY PAD

by CellPath Ltd

Identity

Trade Name
BIOPAD BIOPSY PAD - BLACK EUDAMED
Device Name
BIOPAD BIOPSY PAD - BLACK EUDAMED
Model / Reference
BIOPAD BIOPSY PAD EUDAMED
EBA-0101-03A EUDAMED

Identifiers

Primary DI / UDI-DI
05056256123838 EUDAMED
Basic UDI-DI
05056256EBA001WD EUDAMED
EMDN Code
W0202050385 LABORATORY INSTRUMENTS FOR MICROSCOPIC INVESTIGATIONS - CONSUMABLES 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

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

Biopad Biopsy Pad - Black 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 c15eea27-3478-409d-88c8-5a70c7ec2157 61 fields · synced Aug 4, 2026