Plethysmograph - ANVISA Registration 80200269010
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 80200269010 and manufactured by GERATHERM RESPIRATORY GMBH. The registration is held by GERATHERM MEDICAL LATIN AMERICA 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., EKOVUK MEDI S.R.O., 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
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Registration Details
80200269010
25351093450202383
05111219000181
Company Information
Dates and Status
Mar 06, 2023
VIGENTE
09/18/2025 19:00:01
Plethysmograph
DISPOSITIVO DE FUNÇÃO PULMONAR
VYAIRE MEDICAL GMBH
80102512071
Jul 09, 2018
Plethysmograph
Platinum Elite™ Series – Cabine Pletismografica
MGC DIAGNOSTICS CORPORATION
81721489006
Aug 18, 2022
Respirometer
RESPIRÔMETRO VENTILÔMETRO
KOKO PFT, LTD
82531179002
Jan 06, 2025
Respirometer
RESPIROMETRO
ANESTHESIA ASSOCIATES, INC.
81868349004
May 22, 2023
Respiratory Gas Analyzer
Dispositivo de Função Pulmonar
VYAIRE MEDICAL GMBH
80102512313
Sep 16, 2019
Pletismografo
VLab
EKOVUK MEDI S.R.O.
83073009001
Jun 16, 2025
Pletismografo
VLab-4000
EKOVUK MEDI S.R.O.
82248019001
Apr 29, 2024
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