FLUIDIL - Indonesia BPOM Medical Device Registration
FLUIDIL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420197. The device is manufactured by SEBIA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PROSPEROUS ADVANCED ERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEBIACountry of Origin
France
Authorized Representative
PT. PROSPEROUS ADVANCED ERAAR Address
RUKO PURI BOTANICAL MEGA KEBON JERUK H.7 NO.17
Registration Date
Aug 12, 2024
Expiry Date
Aug 31, 2025
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
SEBIA Antisera K & L Free Light Chains
CSF Control
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 PT M
DIAGNOSTICA STAGO S.A.S
STAGO sthemO VWF Cal
DIAGNOSTICA STAGO S.A.S
STHEMO Thrombin M
DIAGNOSTICA STAGO S.A.S
STAGO sthemO Unical
DIAGNOSTICA STAGO S.A.S
SD lnnovation TA-4V Aggregometer
SD INNOVATION S.A.S
STAGO sthemO CaCl2 M
DIAGNOSTICA STAGO S.A.S
STHEMO PTT A
DIAGNOSTICA STAGO S.A.S
sthemO Fib M
DIAGNOSTICA STAGO S.A.S
Stago Themo Oren Kaler M
DIAGNOSTICA STAGO S.A.S
SEBIA Antisera K & L Free Light Chains
SEBIA