ONE LAMBDA Lyophilized Class I Complement - Indonesia BPOM Medical Device Registration
ONE LAMBDA Lyophilized Class I Complement is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304024810. The device is manufactured by ONE LAMBDA INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ONE LAMBDA INC.Country of Origin
United States
Authorized Representative
SETIA GUNA MEDIKAAR Address
KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT
Registration Date
Dec 17, 2021
Expiry Date
Dec 31, 2024
Product Type
Immunology Laboratory Equipment and Reagents
Complement reagent.
Invitro Diagnostics
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LABScreen ™ Negative Control
Lyophilized Class II Complement
Lyophilized Class I Complement
ONE LAMBDA Terasaki HLA Class I Asian Dry Tissue Typing Tray
LABScreen Single Antigen HLA Class I - Combi
FORTRESS Salmonella Paratyphi AH
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FORTRESS Polyspecific AHG
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FORTRESS Rheumatoid Factors (RF) Latex Test
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Luminex Sheath Fluid - 20 liters
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LABScan 3D Performance Verification Kit
LUMINEX CORP
LABScan 3D Calibration Kit
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BioCore COVID-19 Fast Real Time PCR Kit
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TELLGEN SARS-CoV-2 Nucleic Acid Detection Kit Based on Cartridge Real-Time PCR platform- N gene and ORF1ab gene
TELLGEN CORPORATION
Lyophilized Class II Complement
ONE LAMBDA INC.
LABTYPE™ PE Conjugated Streptavidin
ONE LAMBDA INC.