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Ise Pufr

EUDAMED

Class A (EU MDR)

Ref 106-001688-99Ref B 01-4171-58

by SKALAB s.r.o.

Identity

Trade Name
ISE PUFR EUDAMED
ISE PUFR, 1 x 5000 ml EUDAMED
Device Name
Alkalický promývací roztok EUDAMED
Model / Reference
106-001688-99 EUDAMED
B 01-4171-58 EUDAMED

Identifiers

Primary DI / UDI-DI
08594214080207 EUDAMED
08594214080061 EUDAMED
Basic UDI-DI
859421408SKAIVDP4 EUDAMED
Direct Marketing DI
08594214080207 EUDAMED
08594214080061 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 Pufr 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

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Manufacturer

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

Sources (2)

  • EUDAMED 150418ba-ec4f-4ecc-8168-6c15438512ed 61 fields · synced Jul 19, 2026
  • EUDAMED fb698088-ff93-40a3-96db-0d5a087fc7fb 61 fields · synced May 19, 2026