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Bisulfite Conversion Kit

EUDAMED

Class A (EU MDR)

Ref BCK-RT50

by EntroGen, Inc.

Identity

Device Name
Bisulfite Conversion Kit EUDAMED
Model / Reference
BCK-RT50 EUDAMED

Identifiers

Primary DI / UDI-DI
05060536830675 EUDAMED
Basic UDI-DI
506053683BCK055 EUDAMED
Direct Marketing DI
05060536830675 EUDAMED
EMDN Code
W01019099 CLINICAL CHEMISTRY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Slovenia 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

Yes

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

Bisulfite Conversion Kit by EntroGen, Inc. — 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
EntroGen, Inc.
EUDAMED SRN
US-MF-000022721
Authorised Representative
TANJA TOPOVSEK S.P. SI-AR-000022518

Sources (1)

  • EUDAMED 31bf3776-50b6-41a0-99f7-a4f9e6593b0f 61 fields · synced Jul 22, 2026