NIPRO Single Patient Dialysis Machine Surdial fleX - Indonesia BPOM Medical Device Registration
NIPRO Single Patient Dialysis Machine Surdial fleX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805520004. The device is manufactured by SHIBUYA CORPORATION MEDICAL EQUIPMENT WAKAMIYA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is Main Wheel Beam.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
Main Wheel BeamAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Jan 03, 2025
Expiry Date
Oct 02, 2029
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
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