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Suction Tube

EUDAMED

Class I (EU MDR)

Ref GL-1022Model SCUTION CANNULAS

by Seven Eight Sirgikal

Identity

Trade Name
SUCTION TUBE EUDAMED
Device Name
SCUTION TUBE EUDAMED
Model / Reference
SCUTION CANNULAS EUDAMED
GL-1022 EUDAMED

Identifiers

Primary DI / UDI-DI
+G276GL10220S EUDAMED
Basic UDI-DI
++G276SUCTIONTUBEDJ EUDAMED
Direct Marketing DI
+G276GL10220S EUDAMED
EMDN Code
L1713 OCULAR IRRIGATION OR SUCTION CANNULAS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Suction Tube by Seven Eight Sirgikal — 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
PK-MF-000009959
Authorised Representative
International Business Compendious of Sweden SE-AR-000001625

Sources (1)

  • EUDAMED 4900c08f-0cb8-43fd-a1aa-3d37dc985488 61 fields · synced Jun 18, 2026