Headlight - ANVISA Registration 80073250020
Access comprehensive regulatory information for Headlight in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80073250020 and manufactured by QED INC.. The registration is held by M Z PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including QED INC., ZUMAX MEDICAL CO, LTD., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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Registration Details
80073250020
25351353552200662
04143267000199
Company Information
Dates and Status
Mar 19, 2007
VIGENTE
09/18/2025 19:00:01
Headlight
FOTOFORO
HEINE OPTOTECHNIK GMBH & CO. KG
10243869007
Jun 27, 2005
Headlight
FOTÓFORO LED
North (Nanjing) Instrument Technology Industries Group (NORTH GROUP)
80235600001
Oct 17, 2011
Headlight
FOTÓFORO LED HEADLIGHT
NANCHANG MICARE MEDICAL EQUIPMENT CO., LTD.
80413800008
Aug 18, 2014
Headlight
FOTÓFORO MD
ZUMAX MEDICAL CO, LTD.
80070210019
Jun 13, 2011
Headlight
FOTOFORO DE LED QED
QED INC.
80073250045
Dec 26, 2011
Fotóforo
FOTÓFORO CIRÚRGICO
MK PRODUTOS PARA SAUDE LTDA
10392999018
Feb 10, 2025
Fotóforo
Fotóforo Ultralight
JP COMERCIO DE EQUIPAMENTOS MEDICOS LTDA
82420410008
Dec 23, 2024
Fotóforo
EyeMag Light II
CARL ZEISS MEDITEC AG
10332030135
Aug 26, 2024
Fotóforo
Surgical Headlight
CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD.
80117581106
Dec 18, 2023
Fotóforo
FOTÓFORO EOS 2.0 UNIVET
UNIVET LOUPES S.P.A.
82395290004
Jun 05, 2023