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KYSELINA JODISTÁ p.a.

EUDAMED

Class A (EU MDR)

Ref 19700-30100

by Ing. Petr Švec - PENTA s.r.o.

Identity

Trade Name
KYSELINA JODISTÁ p.a. EUDAMED
Device Name
KYSELINA JODISTÁ p.a. EUDAMED
Model / Reference
19700-30100 EUDAMED

Identifiers

Primary DI / UDI-DI
08595142252506 EUDAMED
Basic UDI-DI
85951422496309W EUDAMED
Direct Marketing DI
08595142252506 EUDAMED
EMDN Code
W01030799 HISTOLOGY / CYTOLOGY 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

Yes

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

KYSELINA JODISTÁ p.a. by Ing. Petr Švec - PENTA 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

EUDAMED SRN
CZ-MF-000035988

Sources (1)

  • EUDAMED 441dafb3-359a-4fc8-b5fa-4fb9500b3ee6 61 fields · synced Jul 9, 2026