Pure Global AI
EUDAMED registration 00180668000168No

6cm ACT Single- INTL

Uromedica, IncorporatedClass IIbEU EUDAMEDTrade name: 6cm ACT Single- INTL
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIb
CND nomenclatures code
P080199
Trade name
6cm ACT Single- INTL
Implantable
Yes
Reusable
No
Measuring function
No
Registration information
Primary DI
00180668000168
Basic UDI
B-00180668000168
Version date
May 14, 2024
Manufacturer last update
June 16, 2023
Active status
No
Manufacturer
Manufacturer name
Uromedica, Incorporated
Country
United States
Country type
NON_EU
Address
1840 Berkshire Lane N Plymouth
Email
info@uromedica-inc.com
Authorized representative
Name
MEDIMARK EUROPE
SRN
FR-AR-000000182
Country
France
Address
11 RUE EMILE ZOLA BP 2332 GRENOBLE cedex 2
Email
info@medimark-europe.com
Telephone
+33 4 76 86 43 22
Regulatory information
Competent authority
Agence Nationale de Sécurité du Médicament et des Produits de Santé
Applicable legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market
France
Market available
Austria:2002-01-01~None, Belgium:2002-01-01~None, Bulgaria:2002-01-01~None, Croatia:2002-01-01~None, Cyprus:2002-01-01~None, Czechia:2002-01-01~None, Denmark:2002-01-01~None, Estonia:2002-01-01~None, Finland:2002-01-01~None, France:2002-01-01~None, Germany:2002-01-01~None, Greece:2002-01-01~None, Hungary:2002-01-01~None, Iceland:2002-01-01~None, Ireland:2002-01-01~None, Italy:2002-01-01~None, Latvia:2002-01-01~None, Liechtenstein:2002-01-01~None, Lithuania:2002-01-01~None, Luxembourg:2002-01-01~None, Malta:2002-01-01~None, Netherlands:2002-01-01~None, Norway:2002-01-01~None, Poland:2002-01-01~None, Portugal:2002-01-01~None, Romania:2002-01-01~None, Slovakia:2002-01-01~None, Slovenia:2002-01-01~None, Spain:2002-01-01~None, Sweden:2002-01-01~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

URINARY INCONTINENCE PROSTHESES - OTHER

About this record

Access comprehensive regulatory information for 6cm ACT Single- INTL in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 00180668000168 and manufactured by Uromedica, Incorporated in United States.

This page provides complete registration details including trade name (6cm ACT Single- INTL), manufacturer information, authorized representative details, competent authority (Agence Nationale de Sécurité du Médicament et des Produits de Santé), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.