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ABX Minotrol Retic

EUDAMED

Class B (EU MDR)

Ref 1300136029Model 2072201, 2072202, 1300136023, 1300136026, 1300136029Ref 1300136026Ref 2072202

by Horiba Abx Sas

Identity

Trade Name
ABX Minotrol Retic EUDAMED
Device Name
ABX Minotrol Retic EUDAMED
Model / Reference
2072201, 2072202, 1300136023, 1300136026, 1300136029 EUDAMED
1300136029 EUDAMED
1300136026 EUDAMED
2072202 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230009734 EUDAMED
03610230009727 EUDAMED
03610230008904 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

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Manufacturer

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (3)

  • EUDAMED 16aaaeda-a8b2-4bc7-98aa-37f83f58de22 61 fields · synced Jul 12, 2026
  • EUDAMED bea43c04-3186-477e-9212-f0f776350c50 61 fields · synced May 16, 2026
  • EUDAMED d054cdbe-d9cc-4086-807f-5ca5782bfec4 61 fields · synced May 17, 2026