ELISIO Synthetic Hemodialyzer - Indonesia BPOM Medical Device Registration
ELISIO Synthetic Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805212412. The device is manufactured by NIPRO CORPORATION ODATE FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO CORPORATION ODATE FACTORYCountry of Origin
Japan
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Aug 31, 2021
Expiry Date
Jul 21, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Non Sterile
ELISIO Synthetic Hemodialyzer
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ELISIO Synthetic Hemodialyzer
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ELISIO Synthetic Hemodialyzer
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ELISIO Synthetic Hemodialyzer
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