Plasma Processing Set - ANVISA Registration 10154450215

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 10154450215 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until Aug 19, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

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10154450215
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Registration Details
ANVISA Registration Number: 10154450215
Janaina dos Santos de Miranda

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Related Devices (2)

Plasmacell-C (Kit descartável para uso com o sistema SpikeSmart)
Risk Class III

Registration Details

10154450215

25351759654202399

49601107000184

Company Information

FRESENIUS KABI AG
Germany
PT: ALEMANHA

Dates and Status

Aug 19, 2024

19/08/2034

09/18/2025 19:00:01

Plasmacell-C (Kit descartável para uso com o sistema SpikeSmart)
Risk Class III

Registration Details

10154450215

25351759654202399

49601107000184

Company Information

Dates and Status

Aug 19, 2024

19/08/2034

09/18/2025 19:00:01

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