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Maxlyte

EUDAMED

Class A (EU MDR)

Ref Maxlyte 3

by Avecon Healthcare Pvt. Ltd.

Identity

Trade Name
MAXLYTE EUDAMED
Device Name
Electrolyte Analyzer EUDAMED
Model / Reference
Maxlyte 3 EUDAMED

Identifiers

Primary DI / UDI-DI
89061707101336 EUDAMED
Basic UDI-DI
890617071AVMAX3JB EUDAMED
EMDN Code
W02010499 BLOOD GAS ANALYSIS / ELECTROLYTE INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Cyprus 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

Yes

EUDAMED

New Device

No

EUDAMED

Maxlyte by Avecon Healthcare Pvt. Ltd. — 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
IN-MF-000040691
Authorised Representative
Amstermed B.V. NL-AR-000001971

Sources (1)

  • EUDAMED 7699a9f8-f8ae-4ee9-894d-a0d6d0b671f2 61 fields · synced Jun 18, 2026