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IOTest 3 Lysing Solution - Indonesia BPOM Medical Device Registration

IOTest 3 Lysing Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320800. The device is manufactured by IMMUNOTECH S.A.S., A BECKMAN COULTER COMPANY. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FOKUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
IOTest 3 Lysing Solution
Analysis ID: AKL 20208320800

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

FOKUS DIAGNOSTIC INDONESIA

AR Address

Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540

Registration Date

Dec 22, 2024

Expiry Date

Dec 31, 2027

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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