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FREND™ COVID-19 Ag+FLU A&B

EUDAMED

Class IVD General (EU MDR)

Ref FRCGFL 020Model FREND™ COVID-19 Ag+FLU A&B

by NanoEntek, Inc.

Identity

Trade Name
FREND™ COVID-19 Ag+FLU A&B EUDAMED
Device Name
FRCGFL 020 EUDAMED
Model / Reference
FREND™ COVID-19 Ag+FLU A&B EUDAMED
FRCGFL 020 EUDAMED

Identifiers

Primary DI / UDI-DI
08809317541013 EUDAMED
Basic UDI-DI
B-08809317541013 EUDAMED
EMDN Code
W0105040504,W0105040699 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

EUDAMEDEUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

FREND™ COVID-19 Ag+FLU A&B 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

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Manufacturer

Manufacturer
NanoEntek, Inc.
EUDAMED SRN
KR-MF-000021903
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 8acc8880-07ea-4986-bbc9-c059e25f187a 61 fields · synced Jun 18, 2026
  • EUDAMED 669fcc6c-5035-442a-aaa0-f86cd59b3c35 61 fields · synced Jun 18, 2026