ANCHOR - ANVISA Registration 80804050316

Access comprehensive regulatory information for ANCHOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80804050316 and manufactured by SMITH E NEPHEW, INC. ENDOSCOPY DIVISION. The registration is held by Smith & Nephew Comércio de Produtos Médicos Ltda. with validity until Sep 06, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including STRYKER ENDOSCOPY, SMITH & NEPHEW INC., ENDOSCOPY DIVISION (ANDOVER), and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80804050316
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Registration Details
ANVISA Registration Number: 80804050316
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

INVISIKNOT - REPARO PARA SINDESMOSE NO TORNOZELO COM FRATURA
Risk Class III

Registration Details

80804050316

25351633984202011

13656820000188

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 06, 2021

06/09/2031

09/18/2025 19:00:01

INVISIKNOT - REPARO PARA SINDESMOSE NO TORNOZELO COM FRATURA
Risk Class III

Registration Details

80804050316

25351633984202011

13656820000188

Company Information

Dates and Status

Sep 06, 2021

06/09/2031

09/18/2025 19:00:01