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S10 Patient Monitor - Indonesia BPOM Medical Device Registration

S10 Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501120140. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH.,LTD.,CHINA from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HOSPI MEDIK INDONESIA.

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 : C
S10 Patient Monitor
Analysis ID: AKL 20501120140

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HOSPI MEDIK INDONESIA

AR Address

Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520

Registration Date

Mar 18, 2021

Expiry Date

Aug 13, 2025

Product Type

Diagnostic Cardiology Equipment

Arrhythmia detector and alarm (including ST-segment measurement and alarm).

Non Radiation Electromedics

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