ANCHOR - ANVISA Registration 80005430360

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 80005430360 and manufactured by STRYKER ENDOSCOPY. The registration is held by STRYKER DO BRASIL LTDA with validity until Feb 18, 2035.

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 SMITH & NEPHEW INC., ENDOSCOPY DIVISION (ANDOVER), STRYKER ENDOSCOPY, 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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80005430360
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Registration Details
ANVISA Registration Number: 80005430360
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

ÂNCORAS EM PEEK TWINLOOP STRYKER
Risk Class III

Registration Details

80005430360

25351181180201423

02966317000102

Company Information

STRYKER ENDOSCOPY
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 18, 2015

18/02/2035

09/18/2025 19:00:01

ÂNCORAS EM PEEK TWINLOOP STRYKER
Risk Class III

Registration Details

80005430360

25351181180201423

02966317000102

Company Information

Dates and Status

Feb 18, 2015

18/02/2035

09/18/2025 19:00:01