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SPIRIT Pulse Oximeter - Indonesia BPOM Medical Device Registration

SPIRIT Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502024639. The device is manufactured by HUNAN ACCURATE BIO-MEDICAL TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN SOURCE MEDICALINDO.

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
SPIRIT Pulse Oximeter
Analysis ID: AKL 20502024639

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MAIN SOURCE MEDICALINDO

AR Address

JL.PROF HM YAMIN SH NO.241 A SEI KERA HILIR I

Registration Date

Jun 24, 2023

Expiry Date

Jun 14, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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DJ Fang

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