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Uromedica, Incorporated devices, product family

by Uromedica, Incorporated 10 variants Basic UDI-DI 0180668000ACTWE

Shared by every variant

Manufacturer
Uromedica, Incorporated(10)
Basic UDI-DI
0180668000ACTWE
Risk class
Class IIb
Legislation
MDD
EMDN category
URINARY INCONTINENCE PROSTHESES - OTHER
Market status
10 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 0180668000ACTWE.

Certificates

1 certificate naming this Basic UDI-DI · EUDAMED

  • G70 045789 0021 Technical documentation · refdata.applicable-legislation.mdr issued
    Notified body 0123 · holder Uromedica, Incorporated · issued 3 Aug 2026 · expires 2 Aug 2031

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 10 devices listed on this page; other pages of the family can carry others.

Variants

10 devices · page 1 of 1

Variants of Uromedica, Incorporated devices, Basic UDI-DI 0180668000ACTWE
UDI-DISize and differences
5cm ACT Double- INTL 800016-01 / 800016-0100180668000052 —On the market
5cm ACT Single- INTL 800021-01 / 800021-0100180668000151 —On the market
6cm ACT Double- INTL 800016-02 / 800016-0200180668000069 —On the market
6cm ACT Single- INTL 800021-02 / 800021-0200180668000168 —On the market
7cm ACT Double- INTL 800016-03 / 800016-0300180668000274 —On the market
7cm ACT Single- INTL 800021-03 / 800021-0300180668000328 —On the market
8cm ACT Double- INTL 800016-04 / 800016-0400180668000281 —On the market
8cm ACT Single- INTL 800021-04 / 800021-0400180668000335 —On the market
9cm ACT Double- INTL 800016-05 / 800016-0500180668000298 —On the market
9cm ACT Single- INTL 800021-05 / 800021-0500180668000342 —On the market