SEBIA Hydragel β1- β2 15 / 30 - Indonesia BPOM Medical Device Registration
SEBIA Hydragel β1- β2 15 / 30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220149. The device is manufactured by SEBIA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is EN. RIOCA MEDICA.
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SEBIA Hydragel β1- β2 15 / 30
Risk Classification
Product Class
Kelas : 2
Manufacturer
SEBIACountry of Origin
France
Authorized Representative
EN. RIOCA MEDICAAR Address
Komplek Pesona Indah Kapuk Blok A6 Jl. Kapuk Kamal Raya Kav. 20A
Registration Date
Feb 05, 2022
Expiry Date
Dec 31, 2024
Product Type
Clinical Chemistry Test System
Protein (fractionation) test system (kit & cair)
Invitro Diagnostics
FLUIDIL
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
Goldsite Hemolysis
GOLDSITE DIAGNOSTICS INC.
GOLDSITE HbA1c Calibrator
GOLDSITE DIAGNOSTICS INC.
GOLDSITE Automatic HPLC HbA1c Analyzer & Accessories
GOLDSITE DIAGNOSTICS INC.
EXIAS e|1 QC-2 Quality Control Level 2
EXIAS MEDICAL GMBH
EXIAS e|1 Analyzer and Accessories
EXIAS MEDICAL GMBH.
EXIAS e|1 Cartridge 600
EXIAS MEDICAL GMBH
EXIAS e|1 QC-1 Quality Control Level 1
EXIAS MEDICAL GMBH.
EXIAS e|1 Cartridge 150
EXIAS MEDICAL GMBH
EXIAS e|1 Cartridge 150 oQC
EXIAS MEDICAL GMBH
EXIAS e|1 Cartridge 300
EXIAS MEDICAL GMBH

