ALVITAL Fingertip Pulse Oximeter - Indonesia BPOM Medical Device Registration
ALVITAL Fingertip Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502120477. The device is manufactured by LEADTEK RESEARCH INC., from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEADTEK RESEARCH INC.,Country of Origin
Taiwan (China)
Authorized Representative
PT. INNOVATION HEALTHCARE INDONESIAAR Address
Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450
Registration Date
Sep 20, 2024
Expiry Date
Nov 17, 2027
Product Type
Monitoring Cardiology Equipment
Oximeter.
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