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Silicone Tube

EUDAMED

Class I (EU MDR)

Ref SRT3001Model Silicone Tube

by Ningbo Luke Medical Devices Co., LTD

Identity

Device Name
Silicone Tube EUDAMED
Model / Reference
Silicone Tube EUDAMED
SRT3001 EUDAMED

Identifiers

Primary DI / UDI-DI
06977523301973 EUDAMED
Basic UDI-DI
697752330SRTW9 EUDAMED
Direct Marketing DI
06977523301973 EUDAMED
EMDN Code
A060102 SURGICAL DRAINAGE CONNECTION MEDICAL TUBES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Silicone Tube by Ningbo Luke Medical Devices Co., LTD — 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-000011732
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 4197517c-3a6e-45f0-98be-05c63658d6ce 61 fields · synced Oct 6, 2026