Intra-Uterine Devices - ANVISA Registration 10208250038
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 10208250038 and manufactured by manufacturer not specified. The registration is held by DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA with validity until Apr 11, 2026.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including PREGNA INTERNATIONAL LIMITED, Meril Endo Surgery Pvt. Ltda, 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.
Related Devices (2)
Registration Details
10208250038
25351206298201590
38756680000140
Company Information
Dates and Status
Apr 11, 2016
11/04/2026
09/18/2025 19:00:01
PREGNA INTERNATIONAL LIMITEDโข India
Meril Endo Surgery Pvt. Ltdaโข India
COOPERSURGICAL INC.โข United States of America
PREGNA INTERNATIONAL LTDโข India
INJEFLEX INDรSTRIA E COMรRCIO DE DISPOSITIVOS E PRODUTOS MรDICOS LTDAโข Brazil
Dispositivos Intra-Uterinos
ANDALAN COPPERFLEX
Not specified
10208250052
Jul 11, 2022
Dispositivos Intra-Uterinos
ANDALAN COPPERFLEX
PREGNA INTERNATIONAL LIMITED
10208250052
Jul 11, 2022
Dispositivos Intra-Uterinos
Dispositivo Intra-uterino MeriTe
Meril Endo Surgery Pvt. Ltda
10360810051
Feb 26, 2020
Dispositivos Intra-Uterinos
Dispositivo Intra-uterino MeriTe
Not specified
10360810051
Feb 26, 2020
Dispositivos Intra-Uterinos
ANDALAN SILVERFLEX
Not specified
10208250037
Feb 22, 2016

