← Back to catalogue

URGO KTwo Reduced

EUDAMED

Class I (EU MDR)

Ref 552898Ref 552903Ref 552899Ref 552902

by Laboratoires Urgo

Identity

Trade Name
URGO KTwo Reduced EUDAMED
URGO KTwo Reduced Latex Free EUDAMED
Device Name
URGO K2 Lite - URGO KTwo Reduced EUDAMED
URGO K2 Lite Latex Free - URGO KTwo Reduced Latex Free EUDAMED
Model / Reference
552898 EUDAMED
552903 EUDAMED
552899 EUDAMED
552902 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890029679 EUDAMED
03546890029624 EUDAMED
03546890029662 EUDAMED
03546890029631 EUDAMED
Basic UDI-DI
354689UM00685J EUDAMED
354689UM00785M EUDAMED
EMDN Code
M03040199 ELASTIC COMPRESSION BANDAGES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMEDEUDAMED

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

URGO KTwo Reduced by Laboratoires Urgo — 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
Laboratoires Urgo
EUDAMED SRN
FR-MF-000002559

Sources (4)

  • EUDAMED 22a572d1-56d6-47cd-be29-e359b5742979 61 fields · synced Aug 3, 2026
  • EUDAMED c76e64d5-5f86-450b-a017-345399b9cee8 61 fields · synced May 17, 2026
  • EUDAMED 12bfdf02-94b0-4dd3-87f3-f831d9ad61c7 61 fields · synced May 17, 2026
  • EUDAMED 90e632d8-13d2-420a-b6de-b43879b19185 61 fields · synced May 18, 2026