I.S.E Pathological Control Serum - Indonesia BPOM Medical Device Registration

I.S.E Pathological Control Serum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208514701. The device is manufactured by I.S.E S.R.L. from Italy, 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

I.S.E Pathological Control Serum

Analysis ID: AKL 20208514701

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

Country of Origin

Italy

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

Mar 23, 2020

Expiry Date

Jan 13, 2025

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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