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Tubes - ANVISA Registration 80825800004

Access comprehensive regulatory information for Tubes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80825800004 and manufactured by SALTER LABS DE MEXICO S.A. DE C.V.. The registration is held by RESPIROX COMÉRCIO DE OXIGÊNIO LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including RICHARD WOLF GMBH, BIOVICO SP. Z O.O., 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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80825800004
2 Related Devices
Registration Details
ANVISA Registration Number: 80825800004
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Related Devices (2)

TUBO SALTER LABS
Risk Class II

Registration Details

80825800004

25351537503201317

74663972000100

Company Information

Mexico
PT: MÉXICO

Dates and Status

Oct 21, 2013

VIGENTE

09/18/2025 19:00:01

TUBO SALTER LABS
Risk Class II

Registration Details

80825800004

25351537503201317

74663972000100

Company Information

SALTER LABS
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 21, 2013

VIGENTE

09/18/2025 19:00:01