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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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BPOM Registered
Risk Class Kelas Resiko : A
LOOPAMP Pure DNA Extraction Kit
Analysis ID: AKL 10204520037

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

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