ANCHOR - ANVISA Registration 10314800157

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 10314800157 and manufactured by GROUPE LÉPINE. The registration is held by ORTOCIR ORTOPEDIA CIRURGIA LTDA with validity until Jan 08, 2028.

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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10314800157
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Registration Details
ANVISA Registration Number: 10314800157
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

ÂNCORA MEMOFIX
Risk Class III

Registration Details

10314800157

25351446338201710

60856937000195

Company Information

GROUPE LÉPINE
France
PT: FRANÇA

Dates and Status

Jan 08, 2018

08/01/2028

09/18/2025 19:00:01

ÂNCORA MEMOFIX
Risk Class III

Registration Details

10314800157

25351446338201710

60856937000195

Company Information

Dates and Status

Jan 08, 2018

08/01/2028

09/18/2025 19:00:01