KIDNY-KLEEN Dialyzer Reprocessor - Indonesia BPOM Medical Device Registration
KIDNY-KLEEN Dialyzer Reprocessor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805110131. The device is manufactured by MEDITOP CO., LTD. from Thailand, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARYATAMA MANDIRI BUSINESS.
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
MEDITOP CO., LTD.Country of Origin
Thailand
Authorized Representative
PT. KARYATAMA MANDIRI BUSINESSAR Address
Komplek Ruko D\'Best Blok B No. 39 Jl. RS Fatmawati No. 15 Gandaria Selatan
Registration Date
Feb 15, 2023
Expiry Date
Dec 19, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Radiation Electromedics
SANKRINA Hemodialysis Bicarbonate
VITAL HEALTHCARE SDN., BHD.
SANKRINA Hemodialysis Bicarbonate
VITAL HEALTHCARE SDN., BHD.
SANKRINA Hollow Fiber Dialyzer (PF Series)
BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
SANKRINA Hollow Fiber Dialyzer (HF Series)
BAIN MEDICAL EQUIPMENT(GUANGZHOU) CO., LTD.
ASAHI Single Patient Dialysis System MDS-101
MED-TECH INC.
SANKRINA Hollow Fiber Dialyzer (H Series)
BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
SANKRINA Hollow Fiber Dialyzer (P Series)
BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
REXEED
ASAHI KASEI MEDICAL MT., CORP.
MDT Plus 4 Cold Sterilant
THAI PEROXIDE CO., LTD.
KIDNY-KLEEN Dialyzer Reprocessor
MEDITOP CO., LTD.