Plasma Processing Set - ANVISA Registration 10154450216
Access comprehensive regulatory information for Plasma Processing Set in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10154450216 and manufactured by manufacturer not specified. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until Mar 10, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including FRESENIUS KABI AG, VIVOSTAT A/S, 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.
Related Devices (2)
Registration Details
10154450216
25351171904202445
49601107000184
Company Information
Dates and Status
Mar 10, 2025
10/03/2035
09/18/2025 19:00:01
Conjunto para Processamento de Plasma
SmartConnect Plasmacell-C
Not specified
10154450217
Aug 04, 2025
Conjunto para Processamento de Plasma
SmartConnect Plasmacell-C
FRESENIUS KABI AG
10154450217
Aug 04, 2025
Conjunto para Processamento de Plasma
Vivostatยฎ Fibrin Sealant
VIVOSTAT A/S
81150729007
Jun 02, 2025
Conjunto para Processamento de Plasma
Plasmacell-C (Kit descartรกvel para uso com o sistema SpikeSmart)
FRESENIUS KABI AG
10154450215
Aug 19, 2024
Conjunto para Processamento de Plasma
Plasmacell-C (Kit descartรกvel para uso com o sistema SpikeSmart)
Not specified
10154450215
Aug 19, 2024

