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Promotor Whole Blood Genomic DNA Extraction Kit

EUDAMED

Class A (EU MDR)

Ref P121-1111-201Ref P121-1211-201

by Acon Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
Promotor Whole Blood Genomic DNA Extraction Kit EUDAMED
Device Name
Whole Blood Genomic DNA Extraction Kit EUDAMED
Model / Reference
P121-1111-201 EUDAMED
P121-1211-201 EUDAMED

Identifiers

Primary DI / UDI-DI
06921756496586 EUDAMED
06921756493653 EUDAMED
Basic UDI-DI
6921756499990017X6 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
Germany 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

Promotor Whole Blood Genomic DNA Extraction Kit by Acon Biotech (Hangzhou) Co., 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-000006977
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED e1c4ad08-7c81-491f-be55-0c70fc6332f2 61 fields · synced Aug 2, 2026
  • EUDAMED 6ad85431-72b6-4ec8-b369-d955006b5c6d 61 fields · synced May 18, 2026