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JUNGSON Centrifuge - Indonesia BPOM Medical Device Registration

JUNGSON Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102220176. The device is manufactured by ZENITH LAB (JIANGSU) CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PURE SOURCE OF ALKESINDO.

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 : B
JUNGSON Centrifuge
Analysis ID: AKL 20102220176

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PURE SOURCE OF ALKESINDO

AR Address

KOMP. PERGUDANGAN PRIMA CENTER 1 EXTENSION F NO 36

Registration Date

Jul 28, 2022

Expiry Date

Apr 23, 2024

Product Type

Clinical Laboratory Equipment

Centrifugal chemistry analyzer for clinical use

Invitro Diagnostics

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