Pure Global AI
ANVISA registration 80077400001Valid until Jan 21, 2027

Devices for Female Contraception

ANVISA Registration Number: 80077400001INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDAINJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDARisk Class IV
Verified
Device names
Technical name
Devices for Female Contraception
View exact technical-name matches →
PT: Dispositivos Para Contracepcao Feminina
Commercial name
DISPOSITIVO INTRAUTERINO DE COBRE
View exact commercial-name matches →
Risk class
Class IV
Registration details
Registration Number
80077400001
Process Number
253510216680122
CNPJ
01997891000165
Company information
Registration Holder
INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA
Manufacturer
INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jan 21, 2002
Validity
21/01/2027
Last Updated
08/18/2026 19:00:00
About this record

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 shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.