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CORNLEY pO2 Electrode - Indonesia BPOM Medical Device Registration

CORNLEY pO2 Electrode is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323642. The device is manufactured by MEIZHOU CORNLEY HI-TECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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BPOM Registered
Risk Class Kelas Resiko : B
CORNLEY pO2 Electrode
Analysis ID: AKL 20101323642

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Aug 11, 2023

Expiry Date

Dec 31, 2025

Product Type

Clinical Chemistry Test System

Blood gases (P CO 2, P O 2) and blood pH test system (kit & cair)

Invitro Diagnostics

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