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DEVICE FOR CLOT REMOVAL - ANVISA Registration 80005430737

Access comprehensive regulatory information for DEVICE FOR CLOT REMOVAL in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80005430737 and manufactured by STRYKER NEUROVASCULAR. The registration is held by STRYKER DO BRASIL LTDA with validity until Dec 13, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ACANDIS GMBH, MICROPORT NEUROTECH (SHANGHAI) CO., LTD, 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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80005430737
2 Related Devices
Registration Details
ANVISA Registration Number: 80005430737
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Related Devices (2)

Dispositivo de Extração ProVue Trevo NXT
Risk Class IV

Registration Details

80005430737

25351160511202163

02966317000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 13, 2021

13/12/2031

09/18/2025 19:00:01

Dispositivo de Extração ProVue Trevo NXT
Risk Class IV

Registration Details

80005430737

25351160511202163

02966317000102

Company Information

Dates and Status

Dec 13, 2021

13/12/2031

09/18/2025 19:00:01