Endoscopic Forceps - ANVISA Registration 80005430037

Access comprehensive regulatory information for Endoscopic Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80005430037 and manufactured by STRYKER ENDOSCOPY. The registration is held by STRYKER DO BRASIL LTDA with validity until Apr 25, 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, RICHARD WOLF GMBH, 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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80005430037
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Registration Details
ANVISA Registration Number: 80005430037
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

PINCAS PEEK CORTANTES PARA CIRURGIAS ENDOSCOPICAS STRYKER
Risk Class III

Registration Details

80005430037

25351010048200328

02966317000102

Company Information

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

Dates and Status

Apr 25, 2003

25/04/2028

09/18/2025 19:00:01

PINCAS PEEK CORTANTES PARA CIRURGIAS ENDOSCOPICAS STRYKER
Risk Class III

Registration Details

80005430037

25351010048200328

02966317000102

Company Information

Dates and Status

Apr 25, 2003

25/04/2028

09/18/2025 19:00:01