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ANVISA registration 10208250052Valid until Jul 11, 2032

Intra-Uterine Devices

ANVISA Registration Number: 10208250052DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDAPREGNA INTERNATIONAL LIMITEDRisk Class IV
Verified
Device names
Technical name
Intra-Uterine Devices
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PT: Dispositivos Intra-Uterinos
Commercial name
ANDALAN COPPERFLEX
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Risk class
Class IV
Registration details
Registration Number
10208250052
Process Number
25351322861202120
CNPJ
38756680000140
Company information
Registration Holder
DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA
Manufacturer
PREGNA INTERNATIONAL LIMITED
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Jul 11, 2022
Validity
11/07/2032
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 10208250052 and manufactured by PREGNA INTERNATIONAL LIMITED. The registration is held by DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA with validity until Jul 11, 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.