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Frend™ Covid-19 Sp
EUDAMEDClass IVD General (EU MDR)
Ref FRCOSW 020Model FREND™ COVID-19 SP
Identity
- Trade Name
- FREND™ COVID-19 SP EUDAMED
- Device Name
- FRCOSW 020 EUDAMED
- Model / Reference
- FREND™ COVID-19 SP EUDAMEDFRCOSW 020 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08809317541082 EUDAMED
- Basic UDI-DI
- B-08809317541082 EUDAMED
- EMDN Code
- W0105040699 VIRAL ANTIGEN/ANTIBODY DETECTION - OTHER EUDAMED
Classification
- Device Class
- Class IVD General 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
Yes
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Frend™ Covid-19 Sp by NanoEnTek, Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-08809317541082 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- NanoEntek, Inc.
- EUDAMED SRN
- KR-MF-000021903
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (1)
- EUDAMED e9bab5f3-d3c9-425d-9164-7ea8c5d50214 61 fields · synced Jul 16, 2026