Plethysmograph - ANVISA Registration 80102512071
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 80102512071 and manufactured by VYAIRE MEDICAL GMBH. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 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.
Device Details
Registration Details
80102512071
25351284832201857
04718143000194
Company Information
Dates and Status
Jul 09, 2018
VIGENTE
09/18/2025 19:00:01
Pletismografo
VLab
EKOVUK MEDI S.R.O.
83073009001
Jun 16, 2025
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

