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Sterile Silicone Tubing

EUDAMED

Class I (EU MDR)

Ref 261-1105-8024-0024

by Medasil Surgical Limited

Identity

Device Name
Sterile Silicone Tubing EUDAMED
Model / Reference
261-1105-8024-0024 EUDAMED

Identifiers

Primary DI / UDI-DI
05060465563934 EUDAMED
Basic UDI-DI
506046556261-11CM EUDAMED
Unit of Use DI
05060465563927 EUDAMED
EMDN Code
A0399 TUBULAR DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sterile Silicone Tubing by Medasil Surgical 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
GB-MF-000009549
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 671ff722-a48f-48cc-bbfc-5dbcee033c87 61 fields · synced Jun 18, 2026