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LABScan 3D Calibration Kit - Indonesia BPOM Medical Device Registration

LABScan 3D Calibration Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103520013. The device is manufactured by LUMINEX CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEGMED DISTRIBUTION INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
LABScan 3D Calibration Kit
Analysis ID: AKL 20103520013

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. SEGMED DISTRIBUTION INDONESIA

AR Address

SEGMED DISTRIBUSI INDONESIA

Registration Date

Jan 20, 2025

Expiry Date

Dec 21, 2027

Product Type

Clinical Toxicology Test System

Clinical toxicology calibrator (kit & cair)

Invitro Diagnostics

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