LOOPAMP Pure DNA Extraction Kit - Indonesia BPOM Medical Device Registration
LOOPAMP Pure DNA Extraction Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204520037. The device is manufactured by EIKEN CHEMICAL CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KIMIA FARMA TBK..
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Risk Classification
Product Class
Kelas : 1
Manufacturer
EIKEN CHEMICAL CO., LTD.Country of Origin
Japan
Authorized Representative
PT. KIMIA FARMA TBK.AR Address
Jalan Veteran No.9 RT.00 /RW.00, Desa/Kelurahan Gambir, Kec. Gambir, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos: 10110
Registration Date
Feb 11, 2025
Expiry Date
Nov 05, 2029
Product Type
Reagents and Specimen Providers
General purpose reagent.
Invitro Diagnostics

