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Cuvette Segments

EUDAMEDFDA UDI

Class A (EU MDR)

Ref A11A01891

by Horiba Abx Sas

Identity

Trade Name
CUVETTE SEGMENTS EUDAMED
CUVETTE SEGMENTS RACK FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
CUVETTE SEGMENTS EUDAMED
Model / Reference
A11A01891 EUDAMED
1220001891 FDA UDI

Identifiers

Primary DI / UDI-DI
03610230005583 EUDAMEDFDA UDI
Basic UDI-DI
361023cuvette_segmentsDE EUDAMED
FDA Product Code
JJE FDA UDI
EMDN Code
W0503010203 SAMPLES ANALYSES, PLASTIC CUVETTES EUDAMED
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2160 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

New Device

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Cuvette Segments by Horiba Abx Sas — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (2)

  • EUDAMED 60f8598e-fe23-41e2-bfc8-482ae29c76d3 61 fields · synced Jul 13, 2026
  • FDA UDI 43b6a1c1-7e4c-4d18-aa03-1f4d8e1eabd2 32 fields · synced May 30, 2026