Pure Global AI
ANVISA registration 10166360071Active

Valve Adjustment Device for Hydrocephalus

ANVISA Registration Number: 10166360071HP BIOPROTESES LTDAHP BIOPROTESES LTDARisk Class I
Verified
Device names
Technical name
Valve Adjustment Device for Hydrocephalus
View exact technical-name matches →
PT: Dispositivo de ajuste de válvula para hidrocefalia
Commercial name
DISPOSITIVO DE REGULAGEM PARA VÁLVULA PROGRAMÁVEL SPHERA PRO – REG-PRO DIGITAL
View exact commercial-name matches →
Risk class
Class I
Registration details
Registration Number
10166360071
Process Number
25351407696202428
CNPJ
54801196000142
Company information
Registration Holder
HP BIOPROTESES LTDA
Manufacturer
HP BIOPROTESES LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Nov 04, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Valve Adjustment Device for Hydrocephalus in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10166360071 and manufactured by HP BIOPROTESES LTDA. The registration is held by HP BIOPROTESES 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.