Identity
- Trade Name
- IRMA ACTH EUDAMED
- Device Name
- IRMA ACTH EUDAMED
- Model / Reference
- IM2030, B89463 EUDAMEDB89463 EUDAMEDIM2030 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 15099590680046 EUDAMED15099590216429 EUDAMED
- Basic UDI-DI
- 150995905ACTHIRMAYL EUDAMED
- EMDN Code
- W0102060401 ADRENOCORTICOTROPIC HORMONE EUDAMED
Classification
- Device Class
- Class C EUDAMED
- Market of Registration
- Czechia 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
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Irma Acth by IMMUNOTECH s.r.o. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 150995905ACTHIRMAYL | Class C | Active |
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Manufacturer
- Manufacturer
- IMMUNOTECH s.r.o.
- EUDAMED SRN
- CZ-MF-000001761
Sources (2)
- EUDAMED 25c2402d-d0f2-4ce9-bc02-3230f94585b0 61 fields · synced Jul 14, 2026
- EUDAMED d42bd04e-81bf-4194-a0cb-0e09a4a049b5 61 fields · synced May 18, 2026