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ANVISA registration 81595559010Active

Flexible Endoscope

ANVISA Registration Number: 81595559010MF MEDICAL - LTDA - MEARTHIMED USA LLCRisk Class II
Verified
Device names
Technical name
Flexible Endoscope
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PT: Endoscopio Flexivel
Commercial name
FAMÍLIA DE ENDOSCOPIO FLEXIVEL ARTHIFLEX
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Risk class
Class II
Registration details
Registration Number
81595559010
Process Number
25351505440202302
CNPJ
13520397000194
Company information
Registration Holder
MF MEDICAL - LTDA - ME
Manufacturer
ARTHIMED USA LLC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Sep 04, 2023
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Flexible Endoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81595559010 and manufactured by ARTHIMED USA LLC. The registration is held by MF MEDICAL - 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.