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ABX Minotrol Retic
EUDAMEDClass B (EU MDR)
Ref 1300136023Model 2072201, 2072202, 1300136023, 1300136026, 1300136029
Identity
- Trade Name
- ABX Minotrol Retic EUDAMED
- Device Name
- ABX Minotrol Retic EUDAMED
- Model / Reference
- 2072201, 2072202, 1300136023, 1300136026, 1300136029 EUDAMED1300136023 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03610230009710 EUDAMED
- Basic UDI-DI
- 361023minotrol_reticB2 EUDAMED
- EMDN Code
- W0103010506 RETICULOCYTE CONTROLS EUDAMED
Classification
- Device Class
- Class B EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
Yes
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
New Device
No
EUDAMED
ABX Minotrol Retic by Horiba Abx Sas — Class B — 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 | 361023minotrol_reticB2 | Class B | Active |
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Manufacturer
- Manufacturer
- Horiba Abx Sas
- EUDAMED SRN
- FR-MF-000000320
Sources (1)
- EUDAMED 1dd339fc-c26a-40bd-ae86-0af8752afc42 61 fields · synced Jun 19, 2026