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Hernia Truss Double-Sided

EUDAMED

Class I (EU MDR)

Ref 2049-BG-L-1Ref 2049-BG-XL-1Ref 2049-BG-M-1Ref 2049-BG-S-1

by OPPO Medical Corp.

Identity

Trade Name
Hernia Truss Double-Sided EUDAMED
Device Name
HERNIA SUPPORTS EUDAMED
Model / Reference
2049-BG-L-1 EUDAMED
2049-BG-XL-1 EUDAMED
2049-BG-M-1 EUDAMED
2049-BG-S-1 EUDAMED

Identifiers

Primary DI / UDI-DI
04719863696966 EUDAMED
04719863696973 EUDAMED
04719863696959 EUDAMED
04719863696942 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

Yes

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 Double-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 (4)

  • EUDAMED ef77f4dc-2ea4-403e-8993-adc0fe8bb7d0 61 fields · synced Sep 17, 2026
  • EUDAMED 7e62a115-9381-408b-a97f-96d79b6983e1 61 fields · synced May 16, 2026
  • EUDAMED 4cb75e8f-6641-4cdc-b1d5-561a257313b0 61 fields · synced May 17, 2026
  • EUDAMED 59263182-af95-4ed8-af2b-fe8ef60e491d 61 fields · synced May 19, 2026