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K3 EDTA/Na Fluoride&gel, glucose level for pregnant women

EUDAMED

Class A (EU MDR)

Ref K3ENFG1307501

by Hygienx Doo Beograd-Rakovica

Identity

Trade Name
K3 EDTA/Na Fluoride&gel, glucose level for pregnant women EUDAMED
Device Name
VACUUM TUBES EUDAMED
Model / Reference
K3ENFG1307501 EUDAMED

Identifiers

Primary DI / UDI-DI
08606034792373 EUDAMED
Basic UDI-DI
8606110811-BLOOD-TUBE-JV EUDAMED
Direct Marketing DI
08606034792373 EUDAMED
EMDN Code
W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Croatia EUDAMED

Clinical & Handling

Sterile

Yes

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

K3 EDTA/Na Fluoride&gel, glucose level for pregnant women by Hygienx Doo Beograd-Rakovica — 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
RS-MF-000048020
Authorised Representative
Salus Cons Kft. HU-AR-000006177

Sources (1)

  • EUDAMED 05d04e27-e624-4dc2-89ce-e18a74cfd8cb 61 fields · synced Oct 6, 2026