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ANVISA registration 10259750030Active

Accessories For Endoscopy

ANVISA Registration Number: 10259750030STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE LTDA.United States Endoscopy Group, Inc. (US Endoscopy)Risk Class II
Verified
Device names
Technical name
Accessories For Endoscopy
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PT: Acessorios Para Endoscopia
Commercial name
Guardus Overtubes
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Risk class
Class II
Registration details
Registration Number
10259750030
Process Number
25351073886202011
CNPJ
59233783000104
Company information
Registration Holder
STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE LTDA.
Manufacturer
United States Endoscopy Group, Inc. (US Endoscopy)
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Feb 26, 2020
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Accessories For Endoscopy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10259750030 and manufactured by United States Endoscopy Group, Inc. (US Endoscopy). The registration is held by STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE 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.