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ANCHOR - ANVISA Registration 80044680485

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 80044680485 and manufactured by CAYENNE MEDICAL, INC.. The registration is held by ZIMMER BIOMET BRASIL LTDA with validity until Mar 29, 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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80044680485
2 Related Devices
Registration Details
ANVISA Registration Number: 80044680485
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Related Devices (2)

Âncoras Quattro GL
Risk Class III

Registration Details

80044680485

25351774159202067

02913684000148

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 29, 2021

29/03/2031

09/18/2025 19:00:01

Âncoras Quattro GL
Risk Class III

Registration Details

80044680485

25351774159202067

02913684000148

Company Information

Dates and Status

Mar 29, 2021

29/03/2031

09/18/2025 19:00:01