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ANVISA registration 80571450003Valid until Oct 13, 2035

Laser System For Therapy

ANVISA Registration Number: 80571450003FISMATEK INDÚSTRIA E COMÉRCIO LTDA - MEBEIJING ADSS DEVELOPMENT CO., LTD.Risk Class III
Verified
Device names
Technical name
Laser System For Therapy
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PT: Sistema de Laser Para Terapia
Commercial name
REVERSI
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Risk class
Class III
Registration details
Registration Number
80571450003
Process Number
25351125556202515
CNPJ
55532188000100
Company information
Registration Holder
FISMATEK INDÚSTRIA E COMÉRCIO LTDA - ME
Manufacturer
BEIJING ADSS DEVELOPMENT CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Oct 13, 2025
Validity
13/10/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Laser System For Therapy in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80571450003 and manufactured by BEIJING ADSS DEVELOPMENT CO., LTD.. The registration is held by FISMATEK INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Oct 13, 2035.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.