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ANVISA registration 80804050351Valid until Aug 07, 2033

Electrosurgical/radiofrequency ablation equipment

ANVISA Registration Number: 80804050351Smith & Nephew Comércio de Produtos Médicos Ltda.ARTHROCARE CORPORATIONRisk Class III
Device names
Technical name
Electrosurgical/radiofrequency ablation equipment
PT: Equipamento de ablação eletrocirúrgica/por radiofrequência
Commercial name
Sistema Werewolf Coblation
Risk class
Class III
Registration details
Registration Number
80804050351
Process Number
25351248104202349
CNPJ
13656820000188
Company information
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 07, 2023
Validity
07/08/2033
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Electrosurgical/radiofrequency ablation equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80804050351 and manufactured by ARTHROCARE CORPORATION. The registration is held by Smith & Nephew Comércio de Produtos Médicos Ltda. with validity until Aug 07, 2033.

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