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Nucleic Acid Extraction Reagent (Swab)

EUDAMED

Class A (EU MDR)

Ref 529007Model 48T/Kit

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Device Name
Nucleic Acid Extraction Reagent (Swab) EUDAMED
Model / Reference
48T/Kit EUDAMED
529007 EUDAMED

Identifiers

Primary DI / UDI-DI
06970341688172 EUDAMED
Basic UDI-DI
69703416803208005JS EUDAMED
Direct Marketing DI
06970341688172 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

Nucleic Acid Extraction Reagent (Swab) by Shenzhen Lifotronic 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-000005654
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED fe1e5a38-67dc-4e25-a83e-edf2f90fc150 61 fields · synced Jun 18, 2026