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Nucleic Acid Extraction Kit
EUDAMEDClass A (EU MDR)
Ref AU18012Model DP4611,DP4612,DP4613,AU17011,AU17012,AU18012,AU18012-96,AU1811,AU1812,AU52111
Identity
- Device Name
- Nucleic Acid Extraction Kit EUDAMED
- Model / Reference
- DP4611,DP4612,DP4613,AU17011,AU17012,AU18012,AU18012-96,AU1811,AU1812,AU52111 EUDAMEDAU18012 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06974541564984 EUDAMED
- Basic UDI-DI
- 697454156002KV EUDAMED
- EMDN Code
- W01019099 CLINICAL CHEMISTRY REAGENTS - OTHER EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Finland 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
No
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Category: Nucleic acid extraction/isolation kit IVD
Nucleic Acid Extraction Kit by Bioteke Corporation (Wuxi) Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Nucleic acid extraction/isolation kit IVD.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 697454156002KV | Class A | Active |
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Manufacturer
- Manufacturer
- BioTeke Corporation（Wuxi）Co., Ltd
- EUDAMED SRN
- CN-MF-000007517
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED b9f1da48-b62f-4beb-8019-e9fbb4686b2c 61 fields · synced Jul 20, 2026