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Eclipse PLUS

EUDAMED

Class A (EU MDR)

Ref M034

by Apex Biotechnology Corp.

Identity

Trade Name
Eclipse PLUS EUDAMED
Device Name
Eclipse PLUS Multi-Purpose Analyzer EUDAMED
Model / Reference
M034 EUDAMED

Identifiers

Primary DI / UDI-DI
04713648762198 EUDAMED
Basic UDI-DI
47136487606B00MCSa73 EUDAMED
Direct Marketing DI
04713648762198 EUDAMED
EMDN Code
W0201060101 GLYCOSILATED HEMOGLOBIN DEVICES 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

Yes

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Eclipse PLUS by Apex Biotechnology Corp. — Class A — 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

EUDAMED SRN
TW-MF-000019773
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED acd03153-079a-4232-b9bb-5e40d81041e6 61 fields · synced Jun 19, 2026