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Succor

EUDAMED

Class IIa (EU MDR)

Ref GS-2115

by Romsons Group Private Limited

Identity

Trade Name
SUCCOR EUDAMED
Device Name
ENDOTRACHEAL TUBE EUDAMED
Model / Reference
GS-2115 EUDAMED

Identifiers

Primary DI / UDI-DI
08907265211504 EUDAMED
Basic UDI-DI
8907265B001YA EUDAMED
EMDN Code
R01030201 ENDOTRACHEAL TUBES, CUFFED, NOT REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Basic endotracheal tube, single-use

Succor by Romsons Group Private Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000036506
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 1271fa85-9e67-472e-8560-44687e9b5fa9 61 fields · synced Jun 18, 2026