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Hernia Truss Single-Sided

EUDAMED

Class I (EU MDR)

Ref 2149-R-BG-S-1

by OPPO Medical Corp.

Identity

Trade Name
Hernia Truss Single-Sided EUDAMED
Device Name
HERNIA SUPPORTS EUDAMED
Model / Reference
2149-R-BG-S-1 EUDAMED

Identifiers

Primary DI / UDI-DI
04719863697024 EUDAMED
Basic UDI-DI
471986369CL110DE EUDAMED
EMDN Code
Y060406 ABDOMINAL HERNIA SUPPORTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

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: Abdominal hernia truss, reusable

Hernia Truss Single-Sided by OPPO Medical Corp. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal hernia truss, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
OPPO Medical Corp.
EUDAMED SRN
TW-MF-000005201
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 1761a203-51aa-466b-884a-e08f17e3d47b 61 fields · synced Jun 19, 2026