Pure Global

PRO LM Pulse Oximeter Fingertip Toscano - Indonesia BPOM Medical Device Registration

PRO LM Pulse Oximeter Fingertip Toscano is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502126864. The device is manufactured by SINO-HERO (SHENZHEN) BIO-MEDICAL ELECTRONICS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
PRO LM Pulse Oximeter Fingertip Toscano
Analysis ID: AKL 20502126864

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Nov 11, 2021

Expiry Date

Aug 25, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from SINO-HERO (SHENZHEN) BIO-MEDICAL ELECTRONICS CO., LTD
Products from the same manufacturer (4 products)