← Back to catalogue

Hernia Truss Double-Sided

EUDAMED

Class I (EU MDR)

Ref 2049-BG-S

by OPPO Medical Inc.

Identity

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

Identifiers

Primary DI / UDI-DI
00840270602401 EUDAMED
Basic UDI-DI
08402706CL1104L EUDAMED
EMDN Code
Y060406 ABDOMINAL HERNIA SUPPORTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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 Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
OPPO Medical Inc.
EUDAMED SRN
US-MF-000005202
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED f0dcc25d-567a-40cc-a059-6590e23c9736 61 fields · synced Jun 18, 2026