Plethysmograph - ANVISA Registration 83073009001
Access comprehensive regulatory information for Plethysmograph in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 83073009001 and manufactured by EKOVUK MEDI S.R.O.. The registration is held by VASCULARTECH COMERCIO, IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS 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 TIMPEL S.A., GERATHERM RESPIRATORY GMBH, 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
Need help with your Brazil registration?
Contact Pure Global Brazil TeamDevice Details
Registration Details
83073009001
25351083125202574
56990683000126
Company Information
Dates and Status
Jun 16, 2025
VIGENTE
09/18/2025 19:00:01
Plethysmograph
VLab-4000
EKOVUK MEDI S.R.O.
82248019001
Apr 29, 2024
Plethysmograph
ENLIGHT
TIMPEL S.A.
81408229003
Jan 21, 2021
Plethysmograph
ENLIGHT
TIMPEL S.A.
81408229002
Apr 06, 2020
Plethysmograph
ENLIGHT 2100
TIMPEL S.A.
81408229004
Mar 25, 2022
Plethysmograph
ENLIGHT 2100
Timpel S.A.
81408229005
Oct 20, 2022
Pletismografo
VLab-4000
EKOVUK MEDI S.R.O.
82248019001
Apr 29, 2024
Pletismografo
Pletismógrafo com difusão
GERATHERM RESPIRATORY GMBH
80200269010
Mar 06, 2023
Pletismografo
ENLIGHT 2100
Timpel S.A.
81408229005
Oct 20, 2022
Pletismografo
Platinum Elite™ Series – Cabine Pletismografica
MGC DIAGNOSTICS CORPORATION
81721489006
Aug 18, 2022
Pletismografo
ENLIGHT 2100
TIMPEL S.A.
81408229004
Mar 25, 2022