← Back to catalogue

Rebound® DUAL

EUDAMED

Class I (EU MDR)

Ref B-242610005Model BU00018

by Össur Iceland ehf.

Identity

Trade Name
Rebound® DUAL EUDAMED
Model / Reference
BU00018 EUDAMED
B-242610005 EUDAMED

Identifiers

Primary DI / UDI-DI
05690977427136 EUDAMED
Basic UDI-DI
5690967BU00018NC EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Rebound® DUAL by Össur Iceland ehf. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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
Össur Iceland ehf.
EUDAMED SRN
IS-MF-000000173

Sources (1)

  • EUDAMED 138fb137-7520-4226-b8f4-4b78c2fc9f96 61 fields · synced Sep 17, 2026