← Back to catalogue

ISE ředící roztok 600 K

EUDAMED

Class A (EU MDR)

Ref P 109.01

by SKALAB s.r.o.

Identity

Trade Name
ISE ředící roztok 600 K EUDAMED
Device Name
Alkalický promývací roztok EUDAMED
Model / Reference
P 109.01 EUDAMED

Identifiers

Primary DI / UDI-DI
08594214080078 EUDAMED
Basic UDI-DI
859421408SKAIVDP4 EUDAMED
Direct Marketing DI
08594214080078 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

Category: Nucleic acid extraction/isolation kit IVD

ISE ředící roztok 600 K by SKALAB s.r.o. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
SKALAB s.r.o.
EUDAMED SRN
CZ-MF-000029744

Sources (1)

  • EUDAMED 15ad3e5d-652d-4111-81f8-f3d87c6569d4 61 fields · synced Jul 31, 2026