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Manufacturer profile

Uromedica, Incorporated

EU EUDAMEDUnited States17 registered devices
VerifiedEUDAMED · official EU database
17
Total devices
2
Risk classes
2024
Earliest version
2024
Latest version
Regulatory footprint
Search Uromedica, Incorporated across other regulatory registries
ThailandColombiaSouth KoreaCanadaEcuadorSaudi Arabia
Recent products (latest 10)
Most recently updated devices in the database
8cm ACT Single- INTL
00180668000335
Class IIb
7cm ACT Single- INTL
00180668000328
Class IIb
6cm ACT Single- INTL
00180668000168
Class IIb
5cm ACT Single- INTL
00180668000151
Class IIb
14cm ProACT Single- INTL
00180668000366
Class IIb
12cm ProACT Single- INTL
00180668000359
Class IIb
9cm ACT Single- INTL
00180668000342
Class IIb
Implantation Instrument Set- INTL
00180668000243
Class I
14cm ProACT Double- INTL
00180668000311
Class IIb
12cm ProACT Double- INTL
00180668000304
Class IIb
Risk class distribution
Breakdown by risk classification
Class IIb1482.4% of total
Class I317.6% of total
Top authorized representatives
Most common authorized representatives for this manufacturer
MEDIMARK EUROPE
100.0%17 devices
About this profile

Explore comprehensive manufacturer profile for Uromedica, Incorporated through Pure Global AI's free EU medical device database. This company manufactures 17 medical devices registered with EUDAMED across 2 risk classes based in United States.

This page provides detailed insights including recent registrations, risk class distribution (Class IIb: 14, Class I: 3), and complete regulatory information from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry.