DIALIFE AV Hemodialysis Tubing Set - Indonesia BPOM Medical Device Registration
DIALIFE AV Hemodialysis Tubing Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220451. The device is manufactured by BAIN MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA KREASI MEDIKA.
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
BAIN MEDICAL EQUIPMENT CO., LTD.Country of Origin
China
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
Hemodialysis system and accessories.
Non Electromedic Sterile
GEKAMED HD - 40 A Hemodialysis Machine
SWS HEMODIALYSIS CARE CO., LTD.
DIALIFE Fistula Needles
DIALIFE SA
DIALIFE Biocart DLC-650
INSPRAMED MEDICAL SAN TIC. A.S.
DAY Hemodialyzer
DIALIFE SA
DIANOVA X2 Hemodialysis Machine
DIALIFE SA
DIANOVA X1 Hemodialysis Machine
SWS HEMODIALYSIS CARE CO., LTD.

