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BIO-FLASH System Rinse

EUDAMED

Class A (EU MDR)

Ref 3000-8205

by Biokit S.A.

Identity

Trade Name
BIO-FLASH System Rinse EUDAMED
Device Name
BIO-FLASH EUDAMED
Model / Reference
3000-8205 EUDAMED

Identifiers

Primary DI / UDI-DI
08426950554462 EUDAMED
Basic UDI-DI
84269506397259T EUDAMED
Direct Marketing DI
08426950554462 EUDAMED
EMDN Code
W0201020185 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - CONSUMABLES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain 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

Yes

EUDAMED

New Device

No

EUDAMED

BIO-FLASH System Rinse by Biokit, S.a. — 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
Biokit S.A.
EUDAMED SRN
ES-MF-000002406

Sources (1)

  • EUDAMED 2bc63a00-f14c-48d0-ae7d-8d6361265f2e 61 fields · synced Jul 24, 2026