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BALIO Calibrator Plus - Indonesia BPOM Medical Device Registration

BALIO Calibrator Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208022239. The device is manufactured by R&D SYSTEMS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.

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BPOM Registered
Risk Class Kelas Resiko : B
BALIO Calibrator Plus
Analysis ID: AKL 20208022239

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

R&D SYSTEMS, INC.

Country of Origin

United States

Authorized Representative

PT. MAIN MEDICAL CHAKRA

AR Address

KOMPLEK GOLDEN BOULEVARD BLOK G2 / 30 BSD CITY KEL. LENGKONG KARYA KEC. SERPONG UTARA TANGERANG SELATAN

Registration Date

Apr 22, 2020

Expiry Date

Feb 05, 2024

Product Type

Hematological Reagents

Calibrator for hemoglobin or hematocrit measurement.

Invitro Diagnostics

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