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Beiwo

EUDAMED

Class A (EU MDR)

Ref BW-MGD2212-A32Model BW-MGD2212-A32 BW-MGD2212-A96

by Hangzhou Beiwo Medical Technology Co., Ltd.

Identity

Trade Name
BEIWO EUDAMED
Device Name
FFPE Tissue gDNA Isolation Kit (Beads) EUDAMED
Model / Reference
BW-MGD2212-A32 BW-MGD2212-A96 EUDAMED
BW-MGD2212-A32 EUDAMED

Identifiers

Primary DI / UDI-DI
06975573960058 EUDAMED
Basic UDI-DI
697557396bwyx005MH EUDAMED
Direct Marketing DI
06975573960058 EUDAMED
EMDN Code
W01019099 CLINICAL CHEMISTRY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

Beiwo by Hangzhou Beiwo Medical Technology 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-000027312
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 70ceceeb-357c-4d13-9011-866a4f2688ac 61 fields · synced Jun 19, 2026