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Neo-Hug Medium

EUDAMED

Class I (EU MDR)

Ref NH-003Model Neo-Hug

by Conlett Technology Inc

Identity

Trade Name
Neo-Hug Medium EUDAMED
Device Name
Neo-Hug EUDAMED
Model / Reference
Neo-Hug EUDAMED
NH-003 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010774 EUDAMED
Basic UDI-DI
697359601Neo-HugQH EUDAMED
Direct Marketing DI
06973596010774 EUDAMED
EMDN Code
V080302 PATIENT POSITIONING MEDICAL CUSHIONS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Neo-Hug Medium by Conlett Technology Inc — 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
CN-MF-000002101
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 0a514ac1-fc2d-4573-8469-66665a585519 61 fields · synced Jun 18, 2026