Intersol Solution - Indonesia BPOM Medical Device Registration
Intersol Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205914132. The device is manufactured by FENWAL FRANCE SAS. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FENWAL FRANCE SAS.Country of Origin
France
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Aug 11, 2023
Expiry Date
May 09, 2028
Product Type
Automatic and Semi-Automatic Hematology Equipment
Multipurpose system for in vitro coagulation studies.
Invitro Diagnostics
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AmiCORE Apheresis Kit - Single Needle with Two Platelet Containers and PAS Connector
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AGILIA SP PCA WIFI ID
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