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Uromedica ACT/ProACT Blunt Trocar

EUDAMED

Class I (EU MDR)

Ref 750022

by Uromedica, Incorporated

Identity

Trade Name
Uromedica ACT/ProACT Blunt Trocar EUDAMED
Device Name
Blunt Trocar- INTL EUDAMED
Model / Reference
750022 EUDAMED

Identifiers

Primary DI / UDI-DI
00180668000250 EUDAMED
Basic UDI-DI
B-00180668000250 EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Surgical retraction system, reusable

Uromedica ACT/ProACT Blunt Trocar by Uromedica, Incorporated — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
US-MF-000008932
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 9f611ba5-18c4-4ad4-a66f-3a396b7bede6 61 fields · synced Jun 17, 2026