DCPro-9 AV Fistula Needles - Indonesia BPOM Medical Device Registration
DCPro-9 AV Fistula Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805126694. The device is manufactured by CHENGDU OCI MEDICAL DEVICES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DIAN CIPTA PHARMINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHENGDU OCI MEDICAL DEVICES CO., LTD.Country of Origin
China
Authorized Representative
PT. DIAN CIPTA PHARMINDOAR Address
PURI SENTRA NIAGA JL WIRALOKA NO 44 BLOK B 44-45. CIPINANG MELAYU. JAKARTA TIMUR
Registration Date
Dec 14, 2023
Expiry Date
Dec 13, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Non Sterile
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