Headlight - ANVISA Registration 10332030135
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 10332030135 and manufactured by CARL ZEISS MEDITEC AG. The registration is held by CARL ZEISS DO BRASIL 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
10332030135
25351366203202492
33131079000149
Company Information
Dates and Status
Aug 26, 2024
VIGENTE
09/18/2025 19:00:01
Headlight
Surgical Headlight
CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD.
80117581106
Dec 18, 2023
Headlight
FOTÓFORO CIRÚRGICO
MK PRODUTOS PARA SAUDE LTDA
10392999018
Feb 10, 2025
Headlight
FOTÓFORO EOS 2.0 UNIVET
UNIVET LOUPES S.P.A.
82395290004
Jun 05, 2023
Headlight
Fotóforo LED para Exames Clínicos Omni MD
BISTOS CO., LTD
80070210092
May 26, 2022
Auxiliary Light
FOCO PARA EXAME LUCEA LED
MAQUET S.A.S.
80259110082
Oct 13, 2014
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
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
Fotóforo
Fotóforo LED para Exames Clínicos Omni MD
BISTOS CO., LTD
80070210092
May 26, 2022