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Im-1080 Tubeguard

EUDAMED

Class I (EU MDR)

Ref IM-1080

by Inoris Medical Sp. Z O.o.

Identity

Trade Name
IM-1080 TUBEGUARD EUDAMED
Device Name
IM-1080 TUBEGUARD EUDAMED
Model / Reference
IM-1080 EUDAMED

Identifiers

Primary DI / UDI-DI
05902596226688 EUDAMED
Basic UDI-DI
B-05902596226688 EUDAMED
EMDN Code
R01038099 ENDOTRACHEAL TUBES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Im-1080 Tubeguard by Inoris Medical Sp. Z O.o. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
PL-MF-000016864

Sources (1)

  • EUDAMED f8c58d06-6108-4110-9345-e7671e1554d6 61 fields · synced Oct 5, 2026