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ELECTROLINE 100 Reagent Pack - Indonesia BPOM Medical Device Registration

ELECTROLINE 100 Reagent Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101222239. The device is manufactured by CARETIUM MEDIACAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HERMAN MEDTEK DIAGNOSTICS.

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BPOM Registered
Risk Class Kelas Resiko : B
ELECTROLINE 100 Reagent Pack
Analysis ID: AKL 20101222239

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HERMAN MEDTEK DIAGNOSTICS

AR Address

Jl. Lingkar Luar Barat, Puri Kembangan, Komplek Rukan Puri Mansion Blok A No.16 Kel.Kembangan Selatan Kec.Kembangan, Kota Jakarta Barat, DKI Jakarta

Registration Date

Dec 16, 2022

Expiry Date

Dec 31, 2025

Product Type

Clinical Chemistry Test System

Calibrator (cair)

Invitro Diagnostics

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