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URGOSTART Tül

EUDAMED

Class IIb (EU MDR)

Ref 754173Ref 754162Ref 754164Ref 754172

by Laboratoires Urgo

Identity

Trade Name
URGOSTART Tül EUDAMED
Device Name
URGOSTART Contact / URGOSTART Interface / URGOSTART Tül EUDAMED
Model / Reference
754173 EUDAMED
754162 EUDAMED
754164 EUDAMED
754172 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890032716 EUDAMED
03546890042166 EUDAMED
03546890042173 EUDAMED
03546890039401 EUDAMED
Basic UDI-DI
354689UM00745D EUDAMED
EMDN Code
M040499 DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

Yes

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: Negative-pressure wound therapy system foam dressing, non-antimicrobial

URGOSTART Tül by Laboratoires Urgo — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Laboratoires Urgo
EUDAMED SRN
FR-MF-000002559

Sources (4)

  • EUDAMED 13c80e06-1660-4775-b41a-bd575dee97c0 61 fields · synced Aug 2, 2026
  • EUDAMED 15dc126b-53a8-4fb7-a562-87aa5fb2c73f 61 fields · synced May 17, 2026
  • EUDAMED b0997a85-a831-4943-8965-d033bbcd9380 61 fields · synced May 18, 2026
  • EUDAMED e95cc273-57bb-4b5d-9ffb-8e78cff038b0 61 fields · synced May 18, 2026