Pure Global AI
ANVISA registration 10259750036Valid until Sep 12, 2036

Polypectomy Snare

ANVISA Registration Number: 10259750036STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE LTDA.United States Endoscopy Group, Inc. (US Endoscopy)Risk Class III
Verified
Device names
Technical name
Polypectomy Snare
View exact technical-name matches →
PT: Alca de Polipectomia
Commercial name
Alças para Polipectomia
View exact commercial-name matches →
Risk class
Class III
Registration details
Registration Number
10259750036
Process Number
25351073378202025
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
Mar 23, 2020
Validity
12/09/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Polypectomy Snare in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10259750036 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 Sep 12, 2036.

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.