DAIWHA Infusion Pump - Indonesia BPOM Medical Device Registration
DAIWHA Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902914768. The device is manufactured by DAIWHA CORP. LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL MEDICAL PRESS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DAIWHA CORP. LTDCountry of Origin
Korea
Authorized Representative
PT. GLOBAL MEDICAL PRESSAR Address
Kompl.Green Garden AA-1/17 Jl.MH Thamrin KM 7 RT 04/RW 02 Kel.Panunggangan Utara Kec.Pinang.Kota Tangerang
Registration Date
Jul 29, 2019
Expiry Date
Mar 05, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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