ANVISA registration 80077400004Valid until Apr 14, 2028Intra-Uterine Devices
ANVISA Registration Number: 80077400004INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDAINJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDARisk Class IV
Device names
- Technical name
- Intra-Uterine Devices
- Commercial name
- DISPOSITIVO INTRAUTERINO DE COBRE OPTIMA DIU ML CU 375
- Risk class
- Class IV
PT: Dispositivos Intra-Uterinos
Registration details
- Registration Number
- 80077400004
- Process Number
- 25351632844200740
- CNPJ
- 01997891000165
Company information
- Registration Holder
- INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA
- Manufacturing Country
- Brazil
PT: BRASIL
Dates and status
- Publication Date
- Apr 14, 2008
- Validity
- 14/04/2028
- Last Updated
- 08/18/2026 19:00:00
About this record
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.
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