ACARE Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration
ACARE Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420161. The device is manufactured by ACARE TECHNOLOGY CO.,LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INMED TEKNOTAMA CEMERLANG.
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
ACARE TECHNOLOGY CO.,LTD.Country of Origin
Taiwan (China)
Authorized Representative
INMED TEKNOTAMA CEMERLANGAR Address
Rukan Inkopau Ujung Menteng Blok B No. 31, Il. Sultan Hamengkubuwono IX Km. 25, Kel. Ujung Menteng Kec. Cakung
Registration Date
Apr 29, 2024
Expiry Date
Dec 14, 2028
Product Type
Monitoring Cardiology Equipment
Oximeter.
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