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Neo-Velum Doublet

EUDAMED

Class I (EU MDR)

Ref NV-DoubletModel Neo-Velum

by Conlett Technology Inc

Identity

Trade Name
Neo-Velum Doublet EUDAMED
Device Name
Neo-Velum EUDAMED
Model / Reference
Neo-Velum EUDAMED
NV-Doublet EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010637 EUDAMED
Basic UDI-DI
697359601Neo-VelumBE EUDAMED
Direct Marketing DI
06973596010637 EUDAMED
EMDN Code
M0303010203 ELASTIC FIXING BANDAGES, SELF-ADHESIVE, EXTENSIBLE IN TWO DIRECTIONS 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-Velum Doublet 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 9087615a-f1d0-4ec2-9c7c-928154d9b150 61 fields · synced Aug 2, 2026