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Blood Collection Tube - Clot Activator

EUDAMED

Class A (EU MDR)

Ref Blood Collection Tube - Clot Activator (Non-Vacuum) (2ML)(PP)

by Nasmed Diagnostic Private Limited

Identity

Device Name
Blood Collection Tube - Clot Activator EUDAMED
Model / Reference
Blood Collection Tube - Clot Activator (Non-Vacuum) (2ML)(PP) EUDAMED

Identifiers

Primary DI / UDI-DI
08906179520948 EUDAMED
Basic UDI-DI
890617952NCLSN EUDAMED
Direct Marketing DI
08906179520948 EUDAMED
EMDN Code
W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

No

EUDAMED

New Device

No

EUDAMED

Blood Collection Tube - Clot Activator by Nasmed Diagnostic Private Limited — 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

EUDAMED SRN
IN-MF-000039587
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED 0bc5abba-6e5f-48b4-883b-e6c45b09db8a 61 fields · synced Jun 18, 2026