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Non Vacuum Blood Collection Tube

EUDAMED

Class A (EU MDR)

Ref Sodium Fluoride 13*75mm 1mlModel No Additive, Clot Activator, Gel & Clot Activator, Sodium Citrate (1:4), Sodium Citrate (1:9), Sodium/Lithium Heparin, EDTA K2/K3, Sodium Fluoride

by Shandong Chengwu Medical Products Factory

Identity

Device Name
Non Vacuum Blood Collection Tube EUDAMED
Model / Reference
No Additive, Clot Activator, Gel & Clot Activator, Sodium Citrate (1:4), Sodium Citrate (1:9), Sodium/Lithium Heparin, EDTA K2/K3, Sodium Fluoride EUDAMED
Sodium Fluoride 13*75mm 1ml EUDAMED

Identifiers

Primary DI / UDI-DI
06973905961674 EUDAMED
Basic UDI-DI
697390596NVBCT018P EUDAMED
EMDN Code
W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

Non Vacuum Blood Collection Tube by Shandong Chengwu Medical Products Factory — 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
CN-MF-000003370
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 3741f722-4652-4c75-b397-c6c686663dc5 61 fields · synced Oct 7, 2026