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CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 80102513494

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 80102513494 and manufactured by APT MEDICAL INC. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Aug 04, 2035.

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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80102513494
2 Related Devices
Registration Details
ANVISA Registration Number: 80102513494
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Related Devices (2)

Fio Guia AnyreachC
Risk Class IV

Registration Details

80102513494

25351418600202457

04718143000194

Company Information

APT MEDICAL INC
China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 04, 2025

04/08/2035

09/18/2025 19:00:01

Fio Guia AnyreachC
Risk Class IV

Registration Details

80102513494

25351418600202457

04718143000194

Dates and Status

Aug 04, 2025

04/08/2035

09/18/2025 19:00:01