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ANVISA registration 81521809001Active

Tracheal Tube

ANVISA Registration Number: 81521809001BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-MEGUANGZHOU AMK MEDICAL EQUIPMENT CO., LTD.Risk Class II
Verified
Device names
Technical name
Tracheal Tube
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PT: Tubo Traqueal
Commercial name
Tubo Endotraqueal Laser
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Risk class
Class II
Registration details
Registration Number
81521809001
Process Number
25351406421202043
CNPJ
27622775000155
Company information
Registration Holder
BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME
Manufacturer
GUANGZHOU AMK MEDICAL EQUIPMENT CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 12, 2020
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Tracheal 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 81521809001 and manufactured by GUANGZHOU AMK MEDICAL EQUIPMENT CO., LTD.. The registration is held by BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME 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.