CSF Control - Indonesia BPOM Medical Device Registration
CSF Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420036. The device is manufactured by SEBIA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PROSPEROUS ADVANCED ERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEBIACountry of Origin
France
Authorized Representative
PROSPEROUS ADVANCED ERAAR Address
RUKO PURI BOTANICAL MEGA KEBON JERUK H.7 NO.17
Registration Date
Apr 30, 2024
Expiry Date
Aug 31, 2025
Product Type
Immunology Laboratory Equipment and Reagents
Immunoelectrophoresis equipment
Invitro Diagnostics
FLUIDIL
SEBIA Antisera K & L Free Light Chains
MINICAP HbA1c
SEBIA Hydrasys 2 Scan Focusing
HYDRAGEL 3 CSF ISOFOCUSING
HYDRASYS Wash Solution
SEBIA Destaining Solution
MINICAP HEMOGLBIN (E)
SEBIA CAPILLARY 3 OCTA
SEBIA HEAD 3 PROTEIN(S) 6
STAGO sthemO VWF Ag
DIAGNOSTICA STAGO S.A.S
STHEMO CK PREST
DIAGNOSTICA STAGO S.A.S
HYDRAGEL 3 CSF ISOFOCUSING
SEBIA
HYDRAGEL 1 THINK JONES
SEBIA
CAPICLEAN
SEBIA
CAPILLARYS 3 WASH SOLUTION
SEBIA
STA Unicalibrator
DIAGNOSTICA STAGO S.A.S.

