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Rapid DNA Extraction kit

EUDAMED

Class A (EU MDR)

Ref 80-07

by Astra Biotech GmbH

Identity

Trade Name
Rapid DNA Extraction kit EUDAMED
Device Name
Rapid DNA Extraction kit EUDAMED
Model / Reference
80-07 EUDAMED

Identifiers

Primary DI / UDI-DI
04251557100675 EUDAMED
Basic UDI-DI
42515571RAPIDDNAUH 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

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

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

Rapid DNA Extraction kit by Astra Biotech GmbH — 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
Astra Biotech GmbH
EUDAMED SRN
DE-MF-000026439

Sources (1)

  • EUDAMED d58bb020-083e-4959-83c0-72dc57ab1674 61 fields · synced Jun 17, 2026