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DNAm Bisulfite Conversion Kit

EUDAMED

Class A (EU MDR)

Ref HBBCModel 50 tests/kit

by Guangzhou Hybribio Medicine Technology Ltd.

Identity

Device Name
DNAm Bisulfite Conversion Kit EUDAMED
Model / Reference
50 tests/kit EUDAMED
HBBC EUDAMED

Identifiers

Primary DI / UDI-DI
06971532201286 EUDAMED
Basic UDI-DI
697153220HBBCEJ EUDAMED
EMDN Code
W0105900101 REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

No

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

DNAm Bisulfite Conversion Kit by Guangzhou Hybribio Medicine Technology Ltd. — 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

EUDAMED SRN
CN-MF-000027677
Authorised Representative
Kingsmead Service B.V. NL-AR-000002066

Sources (1)

  • EUDAMED 67cacccb-2360-4a16-afdd-04cde45f7ef6 61 fields · synced Jul 18, 2026