Intra-Uterine Devices - ANVISA Registration 80077400004
Access comprehensive regulatory information for Intra-Uterine Devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80077400004 and manufactured by INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA. The registration is held by INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA with validity until Apr 14, 2028.
This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including PREGNA INTERNATIONAL LIMITED, Meril Endo Surgery Pvt. Ltda, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
80077400004
25351632844200740
01997891000165
Company Information
Dates and Status
Apr 14, 2008
14/04/2028
09/18/2025 19:00:01
Dispositivos Intra-Uterinos
ANDALAN COPPERFLEX
Not specified
10208250052
Jul 11, 2022
Dispositivos Intra-Uterinos
ANDALAN COPPERFLEX
PREGNA INTERNATIONAL LIMITED
10208250052
Jul 11, 2022
Dispositivos Intra-Uterinos
Dispositivo Intra-uterino MeriTe
Meril Endo Surgery Pvt. Ltda
10360810051
Feb 26, 2020
Dispositivos Intra-Uterinos
Dispositivo Intra-uterino MeriTe
Not specified
10360810051
Feb 26, 2020
Dispositivos Intra-Uterinos
ANDALAN CLASSIC
Not specified
10208250038
Apr 11, 2016

