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ANVISA registration 80071260383Valid until Oct 09, 2027

Multimodality diagnostic X-ray system, mobile

ANVISA Registration Number: 80071260383GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDAGE OEC MEDICAL SYSTEMS INC.Risk Class III
Verified
Device names
Technical name
Multimodality diagnostic X-ray system, mobile
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PT: Sistema de raios-X de diagnóstico multimodalidade, móvel
Commercial name
Sistema de Raio-X com Arco em C Móvel
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Risk class
Class III
Registration details
Registration Number
80071260383
Process Number
25351370335201751
CNPJ
00029372000140
Company information
Registration Holder
GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDA
Manufacturer
GE OEC MEDICAL SYSTEMS INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Oct 09, 2017
Validity
09/10/2027
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Multimodality diagnostic X-ray system, mobile in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80071260383 and manufactured by GE OEC MEDICAL SYSTEMS INC.. The registration is held by GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDA with validity until Oct 09, 2027.

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.