Devices for Female Contraception - ANVISA Registration 80117580783
Access comprehensive regulatory information for Devices for Female Contraception in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80117580783 and manufactured by manufacturer not specified. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Jun 17, 2029.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SEMINA INDÚSTRIA E COMÉRCIO LTDA, INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS 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.
Related Devices (2)
Registration Details
80117580783
25351675437201880
04967408000198
Company Information
Dates and Status
Jun 17, 2019
17/06/2029
09/18/2025 19:00:01
Dispositivos Para Contracepcao Feminina
ANDALAN CAYA® GEL
Not specified
10208250051
Apr 25, 2022
Dispositivos Para Contracepcao Feminina
ANDALAN CAYA® GEL
DELTAMED GMBH
10208250051
Apr 25, 2022
Dispositivos Para Contracepcao Feminina
ANDALAN CAYA® Diafragma
KESSEL MEDINTIM GMBH
10208250050
Mar 28, 2022
Dispositivos Para Contracepcao Feminina
ANDALAN CAYA® Diafragma
Not specified
10208250050
Mar 28, 2022
Dispositivos Para Contracepcao Feminina
Librene
Not specified
80117580797
Jul 01, 2019

