Guide Wire - ANVISA Registration 10315990074
Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10315990074 and manufactured by GTA SRL. The registration is held by NANCY MORAES GOMES LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, 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, SP MEDICAL A/S, 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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Registration Details
10315990074
25351699279201013
00165457000156
Company Information
Dates and Status
Feb 22, 2011
VIGENTE
09/18/2025 19:00:01
Guide Wire
GUIA URETERAL HIDROFÍLICA GTA
GTA SRL
80438830003
Sep 22, 2014
Guide Wire
GUIA URETERAL GTA
GTA SRL
80438830001
Sep 22, 2014
Guide Wire
GUIA URETERAL GTA
GTA SRL
10315990072
Nov 30, 2010
Guide Wire
fio guia hidrofilico urolline
HUNAN REBORN MEDICAL SCIENCE AND TECHNOLOGY DEVELOPMENT CO., LTD
80421079005
Jan 07, 2021
Guide Wire
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10330719033
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E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME• Brazil
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SHUNMEI MEDICAL Co., Ltd• China
SHENZHEN MICROAPPROACH MEDICAL TECHNOLOGY CO., LTD.• China
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SUPERGET FIO GUIA SUPER RÍGIDO
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