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ANVISA registration 10208250050Valid until Mar 28, 2032

Devices for Female Contraception

ANVISA Registration Number: 10208250050DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDAKESSEL MEDINTIM GMBHRisk Class III
Verified
Device names
Technical name
Devices for Female Contraception
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PT: Dispositivos Para Contracepcao Feminina
Commercial name
ANDALAN CAYA® Diafragma
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Risk class
Class III
Registration details
Registration Number
10208250050
Process Number
25351300885202128
CNPJ
38756680000140
Company information
Registration Holder
DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA
Manufacturer
KESSEL MEDINTIM GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Mar 28, 2022
Validity
28/03/2032
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 III medical device is registered under ANVISA number 10208250050 and manufactured by KESSEL MEDINTIM GMBH. The registration is held by DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA with validity until Mar 28, 2032.

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.