← Back to catalogue

Kemilo FT3 Control

EUDAMED

Class IVD General (EU MDR)

Ref CC015MRef CC015HRef CC015L

by Goldsite Diagnostics Inc.

Identity

Trade Name
Kemilo FT3 Control EUDAMED
Device Name
Kemilo FT3 Control EUDAMED
Model / Reference
CC015M EUDAMED
CC015H EUDAMED
CC015L EUDAMED

Identifiers

Primary DI / UDI-DI
06971225936938 EUDAMED
06971225936945 EUDAMED
06971225936921 EUDAMED
Basic UDI-DI
B-06971225936938 EUDAMED
B-06971225936945 EUDAMED
B-06971225936921 EUDAMED
EMDN Code
W0102152002 HORMONE CONTROLS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Kemilo FT3 Control by Goldsite Diagnostics 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001353
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (3)

  • EUDAMED a16d248b-e3a9-4666-bb03-5f14d2c6982d 61 fields · synced Jul 29, 2026
  • EUDAMED 29b428b0-0fec-434b-80bd-45a6304db965 61 fields · synced May 17, 2026
  • EUDAMED 5748ba19-1def-4e32-aef7-0d6e5e30c9b5 61 fields · synced May 18, 2026