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TUD NaF+EDTA

EUDAMED

Class A (EU MDR)

Ref 161009014AModel GLUCOSERef 161008014A

by Tud Sdn Bhd

Identity

Trade Name
TUD NaF+EDTA EUDAMED
TUD NaF+EDTA 8ml EUDAMED
Model / Reference
GLUCOSE EUDAMED
161009014A EUDAMED
161008014A EUDAMED

Identifiers

Primary DI / UDI-DI
09555984601817 EUDAMED
09555984601800 EUDAMED
Basic UDI-DI
955598460GLUCOSEB5 EUDAMED
EMDN Code
W050301020101 SAMPLES ANALYSES, PLASTIC TUBES WITH ADDITIVES EUDAMED

Classification

Device Class
Class A 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

Category: General specimen collection kit

TUD NaF+EDTA by Tud Sdn Bhd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General specimen collection kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Tud Sdn Bhd
EUDAMED SRN
MY-MF-000050104
Authorised Representative
P&J PTE OÜ EE-AR-000049689

Sources (2)

  • EUDAMED 95cc0d5d-19d3-43c8-bb89-4b939b3d6cb6 61 fields · synced Jul 19, 2026
  • EUDAMED f56e4232-3780-42b3-8b28-08499c7af210 61 fields · synced May 19, 2026