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ANVISA registration 82568320015Valid until Nov 03, 2035

LEISHMANIA SP

ANVISA Registration Number: 82568320015GLOBALX PHARMA LTDA.ZHEJIANG ORIENT GENE BIOTECH CO., LTD.Risk Class III
Verified
Device names
Technical name
LEISHMANIA SP
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Commercial name
Teste Rápido em Cassete Leishmania Ab GlobalX
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Risk class
Class III
Registration details
Registration Number
82568320015
Process Number
25351083761202504
CNPJ
41775241000190
Company information
Registration Holder
GLOBALX PHARMA LTDA.
Manufacturer
ZHEJIANG ORIENT GENE BIOTECH CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 03, 2025
Validity
03/11/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for LEISHMANIA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82568320015 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by GLOBALX PHARMA LTDA. with validity until Nov 03, 2035.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.