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CORNLEY pCO2 Buffer - Indonesia BPOM Medical Device Registration

CORNLEY pCO2 Buffer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102320531. The device is manufactured by MEIZHOU CORNLEY HI-TECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
CORNLEY pCO2 Buffer
Analysis ID: AKL 10102320531

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

May 30, 2023

Expiry Date

Dec 31, 2025

Product Type

Clinical Laboratory Equipment

General purpose laboratory equipment labeled or promoted for a specific medical use.

Invitro Diagnostics

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DJ Fang

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