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Hemolyzační promývací roztok 80 H, 100 x 1 ml, Z

EUDAMED

Class A (EU MDR)

Ref P 213.02.ZRef P 213.02

by SKALAB s.r.o.

Identity

Trade Name
Hemolyzační promývací roztok 80 H, 100 x 1 ml, Z EUDAMED
Hemolyzační promývací roztok 80 H EUDAMED
Device Name
Alkalický promývací roztok EUDAMED
Model / Reference
P 213.02.Z EUDAMED
P 213.02 EUDAMED

Identifiers

Primary DI / UDI-DI
08594214080221 EUDAMED
08594214080054 EUDAMED
Basic UDI-DI
859421408SKAIVDP4 EUDAMED
Direct Marketing DI
08594214080221 EUDAMED
08594214080054 EUDAMED
EMDN Code
W01019099 CLINICAL CHEMISTRY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Czechia 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

No

EUDAMED

Companion Diagnostics

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Hemolyzační promývací roztok 80 H, 100 x 1 ml, Z by SKALAB s.r.o. — 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
SKALAB s.r.o.
EUDAMED SRN
CZ-MF-000029744

Sources (2)

  • EUDAMED 42dc309e-e270-4156-99e1-f9765e9e1d27 61 fields · synced Oct 5, 2026
  • EUDAMED 5542ebf9-9eb7-4c12-9df0-ad6ee7b20630 61 fields · synced May 18, 2026