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ANVISA registration 80588390009Active

Reinfusion Bag

ANVISA Registration Number: 80588390009ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE LTDAPuregraft LLCRisk Class II
Verified
Device names
Technical name
Reinfusion Bag
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PT: Bolsa Para Reinfusao
Commercial name
Puregraft 50
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Risk class
Class II
Registration details
Registration Number
80588390009
Process Number
25351061845201931
CNPJ
08290164000102
Company information
Registration Holder
ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE LTDA
Manufacturer
Puregraft LLC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 22, 2019
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Reinfusion Bag in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80588390009 and manufactured by Puregraft LLC. The registration is held by ESTABLISHMENT LABS BRASIL PRODUTOS PARA SAUDE 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.