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ANVISA registration 80003610619Active

FLOW CYTOMETRY - COMPLEMENTARY REAGENTS

ANVISA Registration Number: 80003610619WERFEN MEDICAL LTDALUMINEX CORPORATIONRisk Class I
Verified
Device names
Technical name
FLOW CYTOMETRY - COMPLEMENTARY REAGENTS
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PT: CITOMETRIA DE FLUXO - REAGENTES COMPLEMENTARES
Commercial name
xMAP® Sheath Fluid PLUS
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Risk class
Class I
Registration details
Registration Number
80003610619
Process Number
25351132126202550
CNPJ
02004662000165
Company information
Registration Holder
WERFEN MEDICAL LTDA
Manufacturer
LUMINEX CORPORATION
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Sep 15, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for FLOW CYTOMETRY - COMPLEMENTARY REAGENTS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80003610619 and manufactured by LUMINEX CORPORATION. The registration is held by WERFEN MEDICAL LTDA with validity until currently active (VIGENTE).

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.