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Romolene

EUDAMED

Class IIa (EU MDR)

Ref GS-4032

by Romsons Group Private Limited

Identity

Trade Name
ROMOLENE EUDAMED
Device Name
NASOGASTRIC TUBE EUDAMED
Model / Reference
GS-4032 EUDAMED

Identifiers

Primary DI / UDI-DI
08907265403275 EUDAMED
08907265403206 EUDAMED
08907265403244 EUDAMED
08907265403251 EUDAMED
Basic UDI-DI
8907265F001Z6 EUDAMED
EMDN Code
G02020101 NASOGASTRIC TUBES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED
Belgium 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

Romolene by Romsons Group Private Limited — Class IIa — 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
IN-MF-000036506
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (4)

  • EUDAMED 1167032a-823d-4b97-9c9c-ce63edbc0bd3 61 fields · synced Sep 18, 2026
  • EUDAMED 4f3c5aa2-14bf-4d01-8c59-762c943e4bdc 61 fields · synced May 17, 2026
  • EUDAMED dda44821-9270-412b-b9e2-05916651257f 61 fields · synced May 18, 2026
  • EUDAMED 0bd0df24-923a-48ee-af21-607ac487a347 61 fields · synced May 19, 2026