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DIESTRO ISE Calibrating Pack - Indonesia BPOM Medical Device Registration

DIESTRO ISE Calibrating Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124491. The device is manufactured by JS MEDICINA ELECTRONICA SLR from Argentina, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CITRAMED INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
DIESTRO ISE Calibrating Pack
Analysis ID: AKL 20101124491

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Argentina

Authorized Representative

PT. CITRAMED INDONESIA

AR Address

Jl. Wahid Hasyim No. 59C, RT 002 RW 023, Ds Ngropoh, Kel. Condongcatur, Kec. Depok, Kab. Sleman, D.I. Yogyakarta

Registration Date

Jul 26, 2021

Expiry Date

Nov 01, 2024

Product Type

Clinical Chemistry Test System

Calibrator (cair)

Invitro Diagnostics

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