Devices for Female Contraception - ANVISA Registration 80077400001
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 80077400001 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 Jan 21, 2027.
This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including SEMINA INDÚSTRIA E COMÉRCIO LTDA, SMB CORPORATION OF INDIA, 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
80077400001
253510216680122
01997891000165
Company Information
Dates and Status
Jan 21, 2002
21/01/2027
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

