PHANTOM - ANVISA Registration 82197089005
Access comprehensive regulatory information for PHANTOM in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82197089005 and manufactured by BRPROBE EQUIPAMENTOS ELETRONICOS LTDA.. The registration is held by BRPROBE EQUIPAMENTOS ELETRONICOS 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 KONEX INDรSTRIA E COMรRCIO LTDA.-EPP, VARIAN MEDICAL SYSTEMS, INC., 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
82197089005
25351699595202121
19251315000130
Company Information
Dates and Status
Jul 08, 2021
VIGENTE
09/18/2025 19:00:01
KONEX INDรSTRIA E COMรRCIO LTDA.-EPPโข Brazil
VARIAN MEDICAL SYSTEMS, INC.โข United States of America
SUN NUCLEAR CORPORATIONโข United States of America
CIRS - COMPUTERIZED IMAGING REFERENCE SYSTEMS INCโข United States of America
MMCONEX PRODUTOS PARA SAUDE LTDA.โข Brazil
PHANTOMA (FANTOMA)
DoseLab Phantom Set
Not specified
10405410049
Feb 17, 2025
PHANTOMA (FANTOMA)
DoseLab Phantom Set
VARIAN MEDICAL SYSTEMS, INC.
10405410049
Feb 17, 2025
PHANTOMA (FANTOMA)
FANTOMAS PARA TESTE DE QUALIDADE DE EQUIPAMENTOS DE ULTRASSOM
KONEX INDรSTRIA E COMรRCIO LTDA.-EPP
10358469010
Jan 23, 2023
PHANTOMA (FANTOMA)
Fantoma de verificaรงรฃo do Mobius (MVP)
VARIAN MEDICAL SYSTEMS, INC.
10405410046
Dec 26, 2022
PHANTOMA (FANTOMA)
Fantoma de verificaรงรฃo do Mobius (MVP)
Not specified
10405410046
Dec 26, 2022

