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Gel - ANVISA Registration 81525090004

Access comprehensive regulatory information for Gel in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81525090004 and manufactured by HENAN KANDGI MEDICAL DEVICES CO. LTD. The registration is held by LIKLUC PUERICULTURA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including RMC - INDÚSTRIA BRASILEIRA DE PRODUTOS MÉDICOS LTDA, HELIANTO FARMACEUTICA LTDA, 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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81525090004
Registration Details
ANVISA Registration Number: 81525090004
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Device Details

ADESIVO REFRESCANTE PARA FEBRE EM GEL
Risk Class I

Registration Details

81525090004

25351674223202019

26090108000106

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Dec 23, 2020

VIGENTE

09/18/2025 19:00:01