Disposable Amniotic Membrane Rupturer - ANVISA Registration 80269339004
Access comprehensive regulatory information for Disposable Amniotic Membrane Rupturer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80269339004 and manufactured by BRIGGS MEDICAL SERVICE COMPANY. The registration is held by HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including KYJ Medical Products Co., Ltd., KOLPLAST CI 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.
Device Details
Registration Details
80269339004
25351069135201111
07424092000186
Company Information
Dates and Status
Jun 13, 2011
VIGENTE
09/18/2025 19:00:01
Rompedor de Membrana Amniotica Descartavel
Rompedor de Membrana Amniótica Tiva
WELLMED INTERNATIONAL INDUSTRIES PVT.LTD.
82757049032
Mar 18, 2024
Rompedor de Membrana Amniotica Descartavel
AmniHook Rompedor de Membrana Amniótica Descartável
ASPEN SURGICAL
80269330031
Mar 13, 2023
Rompedor de Membrana Amniotica Descartavel
ROMPEDOR DE BOLSA
KOLPLAST CI LTDA
10237610199
Mar 18, 2019
Rompedor de Membrana Amniotica Descartavel
ROMPEDOR DE BOLSA DESCARTÁVEL
BIOMEDICA - ESTEVES & ANJOS LTDA
10442369004
Mar 06, 2019
Rompedor de Membrana Amniotica Descartavel
Rompedor de Membrana Amniótica Foyomed
NINGBO FOYOMED MEDICAL INSTRUMENTS CO., LTD.
10150479078
Jan 29, 2018

