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ANCHOR - ANVISA Registration 80804050340

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 80804050340 and manufactured by ARTHROCARE CORPORATION. The registration is held by Smith & Nephew Comércio de Produtos Médicos Ltda. with validity until Apr 24, 2033.

This page provides complete technical specifications for 3 related devices, regulatory compliance details, 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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80804050340
3 Related Devices
Registration Details
ANVISA Registration Number: 80804050340
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Related Devices (3)

FAST-FIX FLEX
Risk Class III

Registration Details

80804050340

25351048014202279

13656820000188

Company Information

Costa Rica
PT: COSTA RICA

Dates and Status

Apr 24, 2023

24/04/2033

09/18/2025 19:00:01

FAST-FIX FLEX
Risk Class III

Registration Details

80804050340

25351048014202279

13656820000188

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 24, 2023

24/04/2033

09/18/2025 19:00:01

FAST-FIX FLEX
Risk Class III

Registration Details

80804050340

25351048014202279

13656820000188

Company Information

Dates and Status

Apr 24, 2023

24/04/2033

09/18/2025 19:00:01