VIKAMED Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration
VIKAMED Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502910072. The device is manufactured by EDAN INSTRUMENTS INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EDAN INSTRUMENTS INC.Country of Origin
China
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
jl.Ciputat Raya no 14 B.Pondok Pinang
Registration Date
Nov 15, 2021
Expiry Date
Nov 15, 2024
Product Type
Monitoring Cardiology Equipment
Oximeter.
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