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JUNGSON Stethoscope - Indonesia BPOM Medical Device Registration

JUNGSON Stethoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10501025223. The device is manufactured by SHANGHAI CAREMATE MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
JUNGSON Stethoscope
Analysis ID: AKL 10501025223

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. PURE SOURCE OF ALKESINDO

AR Address

KOMP. PERGUDANGAN PRIMA CENTER 1 EXTENSION F NO 36

Registration Date

Sep 12, 2020

Expiry Date

Apr 23, 2024

Product Type

Diagnostic Cardiology Equipment

Stethoscope.

Non Electromedic Non Sterile

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