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Neo-Shield

EUDAMED

Class I (EU MDR)

Ref Ref-002Model Neo-Shield

by Conlett Technology Inc

Identity

Trade Name
Neo-Shield EUDAMED
Device Name
Neo-Shield EUDAMED
Model / Reference
Neo-Shield EUDAMED
Ref-002 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010453 EUDAMED
Basic UDI-DI
697359601Neo-ShieldBJ EUDAMED
Direct Marketing DI
06973596010453 EUDAMED
EMDN Code
T030199 COVERS, INSTRUMENTS AND EQUIPMENT - OTHER 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-Shield 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 a84e1f64-5bc4-4ae7-a62a-3a7128f4f101 61 fields · synced Jul 9, 2026