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Blood Collection Tube - Lithium Heparin

EUDAMED

Class A (EU MDR)

Ref Blood Collection Tube - Lithium Heparin (Non-Vacuum) (3ML)(PP)

by Nasmed Diagnostic Private Limited

Identity

Device Name
Blood Collection Tube - Lithium Heparin EUDAMED
Model / Reference
Blood Collection Tube - Lithium Heparin (Non-Vacuum) (3ML)(PP) EUDAMED

Identifiers

Primary DI / UDI-DI
08906179521044 EUDAMED
Basic UDI-DI
890617952NLHT9 EUDAMED
Direct Marketing DI
08906179521044 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 - Lithium Heparin 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

Manufacturer
Nasmed Diagnostic Private Limited
EUDAMED SRN
IN-MF-000039587
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED 4b7263f3-f473-44f7-a584-c8ae69254dcf 61 fields · synced Jun 19, 2026