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DCPro-9 Low Flux Polyethersulfone Hollow Fiber Hemodialyzer - Indonesia BPOM Medical Device Registration

DCPro-9 Low Flux Polyethersulfone Hollow Fiber Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805127744. 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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BPOM Registered
Risk Class Kelas Resiko : C
DCPro-9 Low Flux Polyethersulfone Hollow Fiber Hemodialyzer
Analysis ID: AKL 20805127744

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DIAN CIPTA PHARMINDO

AR Address

PURI SENTRA NIAGA JL WIRALOKA NO 44 BLOK B 44-45. CIPINANG MELAYU. JAKARTA TIMUR

Registration Date

Dec 08, 2023

Expiry Date

Dec 07, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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