← Back to catalogue

Su-40

EUDAMED

Class A (EU MDR)

Ref 904-0721-9

by Sysmex Corporation

Identity

Trade Name
SU-40 EUDAMED
Device Name
REACTION TUBE EUDAMED
Model / Reference
904-0721-9 EUDAMED

Identifiers

Primary DI / UDI-DI
04987562516896 EUDAMED
04987562200139 EUDAMED
Basic UDI-DI
4987562SU-406H EUDAMED
EMDN Code
W0503010203 SAMPLES ANALYSES, PLASTIC CUVETTES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

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

Su-40 by Sysmex Corporation — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sysmex Corporation
EUDAMED SRN
JP-MF-000014037
Authorised Representative
Sysmex Europe SE DE-AR-000022333

Sources (2)

  • EUDAMED 47281eeb-3492-48f9-8122-300c3de1749a 61 fields · synced Jul 27, 2026
  • EUDAMED 1eb2c8d0-573c-4119-92f7-d80495505aed 61 fields · synced May 19, 2026