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ANVISA registration 83368109006Active

Cold Light Source

ANVISA Registration Number: 83368109006TRANSMEDX HEALTHCARE COMERCIO E SERVICOS LTDAGENESIS MEDTECH SURGICAL DEVICE (WUXI) CO., LTDRisk Class II
Verified
Device names
Technical name
Cold Light Source
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PT: Fonte de Luz Fria
Commercial name
Fonte de Iluminação Endoscópica Genesis
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Risk class
Class II
Registration details
Registration Number
83368109006
Process Number
25351113609202636
CNPJ
60132904000100
Company information
Registration Holder
TRANSMEDX HEALTHCARE COMERCIO E SERVICOS LTDA
Manufacturer
GENESIS MEDTECH SURGICAL DEVICE (WUXI) CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jul 13, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Cold Light Source in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 83368109006 and manufactured by GENESIS MEDTECH SURGICAL DEVICE (WUXI) CO., LTD. The registration is held by TRANSMEDX HEALTHCARE COMERCIO E SERVICOS LTDA with validity until currently active (VIGENTE).

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.