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CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 81667100040

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81667100040 and manufactured by Shanghai MicroPort Medical (Group) Co., Ltd. The registration is held by MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA with validity until Oct 26, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ABBOTT MEDICAL, COOK INCORPORATED, 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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81667100040
2 Related Devices
Registration Details
ANVISA Registration Number: 81667100040
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Related Devices (2)

Fio Guia Hidrofรญlico
Risk Class IV

Registration Details

81667100040

25351391970202014

29182018000133

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

Oct 26, 2020

26/10/2030

09/18/2025 19:00:01

Fio Guia Hidrofรญlico
Risk Class IV

Registration Details

81667100040

25351391970202014

29182018000133

Company Information

Dates and Status

Oct 26, 2020

26/10/2030

09/18/2025 19:00:01