Vena Cava Filter - ANVISA Registration 80102510930
Access comprehensive regulatory information for Vena Cava Filter in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80102510930 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Feb 22, 2036.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including B. BRAUN MEDICAL, LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD., 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
80102510930
25351328609201037
04718143000194
Company Information
Dates and Status
Feb 22, 2011
22/02/2036
09/18/2025 19:00:01
Filtro Venoso
SISTEMA DE FILTRO DE VEIA CAVA FITAYA
Not specified
80102513074
Aug 21, 2023
Filtro Venoso
SISTEMA DE FILTRO DE VEIA CAVA FITAYA
LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.
80102513074
Aug 21, 2023
Filtro Venoso
VENATECH® RETRIEVABLE
B. BRAUN MEDICAL
80136990863
Dec 05, 2016
Filtro Venoso
VENATECH® RETRIEVABLE
Not specified
80136990863
Dec 05, 2016
Filtro Venoso
VENATECH CONVERTIBLE
Not specified
80136990552
Jan 28, 2008

