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ANVISA registration 82738739003Active

Endobronchial Tube

ANVISA Registration Number: 82738739003BROOK S/AROYAL FORNIA MEDICAL EQUIPMENT CO., LTD.Risk Class II
Verified
Device names
Technical name
Endobronchial Tube
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PT: Tubo Endobronquial
Commercial name
Tubo Endobronquial Duplo Lúmen Brook
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Risk class
Class II
Registration details
Registration Number
82738739003
Process Number
25351795662202307
CNPJ
05490655000109
Company information
Registration Holder
BROOK S/A
Manufacturer
ROYAL FORNIA MEDICAL EQUIPMENT CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Dec 11, 2023
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Endobronchial Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82738739003 and manufactured by ROYAL FORNIA MEDICAL EQUIPMENT CO., LTD.. The registration is held by BROOK S/A 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.