DIALIFE Biocart DLC-650 - Indonesia BPOM Medical Device Registration
DIALIFE Biocart DLC-650 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220452. The device is manufactured by INSPRAMED MEDICAL SAN TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA KREASI MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INSPRAMED MEDICAL SAN TIC. A.S.Country of Origin
Turkey
Authorized Representative
PT. GRAHA KREASI MEDIKAAR Address
Pakuwon Tower Kota Kasablanka Lt. 10 Unit J, Jl.Casablanca No. 88
Registration Date
Nov 25, 2022
Expiry Date
Oct 31, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
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