CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 81576620001
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 81576620001 and manufactured by manufacturer not specified. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Jul 14, 2028.
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.
Related Devices (2)
Registration Details
81576620001
25351102608202313
27548227000122
Company Information
Dates and Status
Mar 06, 2023
14/07/2028
09/18/2025 19:00:01
ABBOTT MEDICALโข United States of America
COOK INCORPORATEDโข United States of America
BOSTON SCIENTIFIC CORPORATION - MARLBOROUGHโข United States of America
BOSTON SCIENTIFIC CORPORATIONโข United States of America
ASAHI INTECC CO.,LTDโข Japan
FIO GUIA CARDIOVASCULAR
Fio Guia AnyreachC
APT MEDICAL INC
80102513494
Aug 04, 2025
FIO GUIA CARDIOVASCULAR
Fio Guia AnyreachC
Not specified
80102513494
Aug 04, 2025
FIO GUIA CARDIOVASCULAR
FIO GUIA CORDIS EMERALD
Not specified
81576620044
May 19, 2025
FIO GUIA CARDIOVASCULAR
FIO GUIA CORDIS EMERALD
CORDIS US CORP.
81576620044
May 19, 2025
FIO GUIA CARDIOVASCULAR
Fio-guia Super Stiff ZoeTrackโข
LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD.
80102513407
Apr 14, 2025

