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ANVISA registration 80239100005Active

Vacuum Regulator

ANVISA Registration Number: 80239100005BIOCATH COMÉRCIO DE PRODUTOS HOSPITALARES LTDAGENTEC (SHANGHAI) CORPORATIONRisk Class I
Verified
Device names
Technical name
Vacuum Regulator
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PT: Regulador de Vacuo
Commercial name
Regulador de sucção da série 882VR
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Risk class
Class I
Registration details
Registration Number
80239100005
Process Number
25351722143202311
CNPJ
05964709000120
Company information
Registration Holder
BIOCATH COMÉRCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
GENTEC (SHANGHAI) CORPORATION
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 20, 2023
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for Vacuum Regulator in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80239100005 and manufactured by GENTEC (SHANGHAI) CORPORATION. The registration is held by BIOCATH COMÉRCIO DE PRODUTOS 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.