ANCHOR - ANVISA Registration 81464750162

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 81464750162 and manufactured by manufacturer not specified. The registration is held by Domo Salute Consultoria Regulatória Ltda with validity until Oct 29, 2034.

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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81464750162
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Registration Details
ANVISA Registration Number: 81464750162
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

BIOTEK Âncora de ligamento PEEK com fibra/fita de fibra [Sem nó - 2 peças de âncora (eyelet em Titânio)]
Risk Class III

Registration Details

81464750162

25351678432202376

26263959000103

Company Information

Dates and Status

Oct 29, 2024

29/10/2034

09/18/2025 19:00:01

BIOTEK Âncora de ligamento PEEK com fibra/fita de fibra [Sem nó - 2 peças de âncora (eyelet em Titânio)]
Risk Class III

Registration Details

81464750162

25351678432202376

26263959000103

Company Information

India
PT: ÍNDIA

Dates and Status

Oct 29, 2024

29/10/2034

09/18/2025 19:00:01