AIMTECH Pulse Oximeter - Indonesia BPOM Medical Device Registration
AIMTECH Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502916540. The device is manufactured by UTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARMICO INTI 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
UTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. ARMICO INTI MEDIKAAR Address
Jl. Bedugul 1A No. 3
Registration Date
Sep 16, 2022
Expiry Date
Sep 15, 2025
Product Type
Monitoring Cardiology Equipment
Oximeter.
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