← Back to catalogue

Progesterone (EECL)

EUDAMED

Class IVD General (EU MDR)

Ref 1030202000Model 50 tests/kitRef 1030211000

by Accucise Diagnostics Inc.

Identity

Device Name
Progesterone (EECL) EUDAMED
Model / Reference
50 tests/kit EUDAMED
1030202000 EUDAMED
1030211000 EUDAMED

Identifiers

Primary DI / UDI-DI
06975090501321 EUDAMED
06975090502328 EUDAMED
Basic UDI-DI
B-06975090501321 EUDAMED
B-06975090502328 EUDAMED
EMDN Code
W0102050106 PROGESTERONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Progesterone (EECL) by Accucise 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-000045017
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (2)

  • EUDAMED 2917910f-b085-4e06-ae8d-28f831ea4ff6 61 fields · synced Jun 20, 2026
  • EUDAMED 3dc258af-b059-4b5b-a854-c9680ec2bbc2 61 fields · synced May 18, 2026