ONEHEALTH Oxygen Regulator - Indonesia BPOM Medical Device Registration
ONEHEALTH Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402124478. The device is manufactured by NINGBO KAIPO ELECTRON INSTRUMENT AND METER CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDICAL ERA ALKESINDO.
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 : 1
Country of Origin
China
Authorized Representative
PT. MEDICAL ERA ALKESINDOAR Address
Jl. Sisingamangaraja Kilometer 10.8, Komplek Amplas Trade Centre Blok Mahoni nomor 08, Kota Medan, Provinsi Sumatera Utara, Kode Pos: 20148
Registration Date
Aug 01, 2024
Expiry Date
Jul 31, 2027
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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ONEHEALTH ANEROID SPHYGMOMANOMETER STANDING
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ONEHEALTH Manual Wheelchair (Anak) OH809
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ONEHEALTH REFLEX HAMMERS
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