ANCHOR - ANVISA Registration 80062900011

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 80062900011 and manufactured by ORTOBIO S.A.. The registration is held by ORTOBIO S.A. with validity until Nov 10, 2033.

This page provides complete technical specifications for this device, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80062900011
Registration Details
ANVISA Registration Number: 80062900011
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

Âncora Rosqueada em Titânio
Risk Class III

Registration Details

80062900011

25351545948200804

03974404000174

Company Information

ORTOBIO S.A.
Brazil
PT: BRASIL

Dates and Status

Nov 10, 2008

10/11/2033

09/18/2025 19:00:01