Apheresis Kit - ANVISA Registration 10077090145
Access comprehensive regulatory information for Apheresis Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10077090145 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until May 04, 2030.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including FRESENIUS KABI AG, HAEMONETICS CORPORATION, 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
10077090145
25351832195202133
49601107000184
Company Information
Dates and Status
Jan 03, 2022
04/05/2030
09/18/2025 19:00:01
Kit para Aferese
Kit de aférese AmiCORE
Not specified
10154450214
Dec 26, 2023
Kit para Aferese
Kit de aférese AmiCORE
FRESENIUS KABI AG
10154450214
Dec 26, 2023
Kit para Aferese
Conjunto de Fotoférese THERAKOS® CELLEX®
Not specified
10234400321
Dec 26, 2022
Kit para Aferese
Conjunto de Fotoférese THERAKOS® CELLEX®
MALLINCKRODT PHARMACEUTICALS IRELAND LIMITED
10234400321
Dec 26, 2022
Kit para Aferese
Conjunto de Fotoférese THERAKOS® CELLEX®
THERAKOS INC.
10234400321
Dec 26, 2022

