DAY Hemodialyzer - Indonesia BPOM Medical Device Registration
DAY Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220401. The device is manufactured by DIALIFE SA from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA KREASI MEDIKA.
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DIA Hemodialyzer
Risk Classification
Product Class
Kelas : 2
Manufacturer
DIALIFE SACountry of Origin
Switzerland
Authorized Representative
PT. GRAHA KREASI MEDIKAAR Address
Pakuwon Tower Kota Kasablanka Lt. 10 Unit J, Jl.Casablanca No. 88
Registration Date
Nov 03, 2022
Expiry Date
Oct 31, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
High permeability hemodialysis system.
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