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Romo Soft

EUDAMED

Class IIa (EU MDR)

Ref GS-2102

by Romsons Group Private Limited

Identity

Trade Name
ROMO SOFT EUDAMED
Device Name
TRACHEOSTOMY TUBE EUDAMED
Model / Reference
GS-2102 EUDAMED

Identifiers

Primary DI / UDI-DI
08907265210279 EUDAMED
Basic UDI-DI
8907265B007YN EUDAMED
EMDN Code
R0105020101 TRACHEOSTOMIC CANNULAS, CUFFED, NOT REINFORCED, WITH FIXED FLANGE, AND KITS 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: Tracheostomy tube, non-reinforced, non-customized, single-use

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

Similar devices

Also classified as Tracheostomy tube, non-reinforced, non-customized, 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 e535430d-696a-4814-b12d-7d021775c2cb 61 fields · synced Jun 18, 2026