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Neolife

EUDAMED

Class I (EU MDR)

Ref FA-012

by Aadhar Medicare Private Limited

Identity

Trade Name
NEOLIFE EUDAMED
Device Name
Fracture Aids EUDAMED
Model / Reference
FA-012 EUDAMED

Identifiers

Primary DI / UDI-DI
08906164421038 EUDAMED
Basic UDI-DI
890616442FAX7 EUDAMED
Direct Marketing DI
08906164421038 EUDAMED
EMDN Code
M030501 IMMOBILISATION BANDAGES FOR SHOULDER, ARM AND COLLARBONE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Neolife by Aadhar Medicare Private Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000034117
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED d8b4e64e-2c2b-4e27-b4da-36b44304a9d0 61 fields · synced Jun 19, 2026