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ANCHOR - ANVISA Registration 80044680494

Access comprehensive regulatory information for ANCHOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80044680494 and manufactured by CAYENNE MEDICAL, INC.. The registration is held by ZIMMER BIOMET BRASIL LTDA with validity until Jun 28, 2031.

This page provides complete technical specifications for 2 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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80044680494
2 Related Devices
Registration Details
ANVISA Registration Number: 80044680494
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Related Devices (2)

Âncoras Biowick X
Risk Class IV

Registration Details

80044680494

25351063971202063

02913684000148

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 28, 2021

28/06/2031

09/18/2025 19:00:01

Âncoras Biowick X
Risk Class IV

Registration Details

80044680494

25351063971202063

02913684000148

Company Information

Dates and Status

Jun 28, 2021

28/06/2031

09/18/2025 19:00:01