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ANVISA registration 80050820009Active

Limb Compression System

ANVISA Registration Number: 80050820009MAX-CIRURGICA Comercio de Materiais Hospitalares LtdaDALIAN LABTEK SCIENCE & DEVELOPMENT CO. LTD.Risk Class II
Verified
Device names
Technical name
Limb Compression System
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PT: Sistema de Compressao de Membros
Commercial name
Veinoflow SCD
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Risk class
Class II
Registration details
Registration Number
80050820009
Process Number
25351360938201864
CNPJ
89982037000176
Company information
Registration Holder
MAX-CIRURGICA Comercio de Materiais Hospitalares Ltda
Manufacturer
DALIAN LABTEK SCIENCE & DEVELOPMENT CO. LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Aug 27, 2018
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Limb Compression System in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80050820009 and manufactured by DALIAN LABTEK SCIENCE & DEVELOPMENT CO. LTD.. The registration is held by MAX-CIRURGICA Comercio de Materiais Hospitalares 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.