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BioSap HS, 500 mL

EUDAMED

Class A (EU MDR)

Ref KS-500

by BioGnost Ltd.

Identity

Trade Name
BioSap HS, 500 mL EUDAMED
Device Name
Dodaci hranjivim podlogama EUDAMED
Model / Reference
KS-500 EUDAMED

Identifiers

Primary DI / UDI-DI
03858892125113 EUDAMED
Basic UDI-DI
385889212BAC4010104SUQL EUDAMED
Direct Marketing DI
03858892125113 EUDAMED
EMDN Code
W0104010104 ADDITIVES FOR DCM (GROWTH SUPPLEMENTS, SELECTIVE AGENTS, ...) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Croatia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

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

BioSap HS, 500 mL by BioGnost Ltd. — 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
BioGnost Ltd.
EUDAMED SRN
HR-MF-000022153

Sources (1)

  • EUDAMED 3e1fb3ac-e338-4cd0-a6d2-08511dde4a25 61 fields · synced Jun 18, 2026