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Extractor - ANVISA Registration 80633660007

Access comprehensive regulatory information for Extractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80633660007 and manufactured by manufacturer not specified. The registration is held by IGI COMERCIO DE EQUIPAMENTOS ELETRONICOS LTDA with validity until Jun 26, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including RUSSER BRASIL LTDA, KARL STORZ SE & CO. KG, 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.

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80633660007
2 Related Devices
Registration Details
ANVISA Registration Number: 80633660007
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Related Devices (2)

KIT DE EXTRAÇÃO E/OU REPOSICIONAMENTO DO FILTRO DE VEIA CAVA OPCIONAL ALN - ALN 2 in 1 RS
Risk Class IV

Registration Details

80633660007

25351037561202318

10394359000144

Company Information

Dates and Status

Jun 26, 2023

26/06/2033

09/18/2025 19:00:01

KIT DE EXTRAÇÃO E/OU REPOSICIONAMENTO DO FILTRO DE VEIA CAVA OPCIONAL ALN - ALN 2 in 1 RS
Risk Class IV

Registration Details

80633660007

25351037561202318

10394359000144

Company Information

ALN S.A.R.L.
France
PT: FRANÇA

Dates and Status

Jun 26, 2023

26/06/2033

09/18/2025 19:00:01