ZENITHT ZEUS Kyphoplasty Balloon Catheter System - Indonesia BPOM Medical Device Registration
ZENITHT ZEUS Kyphoplasty Balloon Catheter System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420188. The device is manufactured by ZENITHT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CHAKRA JAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZENITHT CO., LTD.Country of Origin
Korea
Authorized Representative
PT. CHAKRA JAYA MEDIKAAR Address
Jl. TB Simatupang Kav. 18/ 18 Office Park Lantai 22 Suites E, F, & G
Registration Date
Jun 01, 2024
Expiry Date
Jan 16, 2029
Product Type
Prosthetic Orthopedic Equipment
Polymethylmethacrylate (PMMA) bone cement.
Non Electromedic Sterile
DESU DECURVE Silicone Shunt
DESU MEDIKAL URUNLER VE TฤฐBBฤฐ CIHAZLAR SAN. VE TIC. A.S.
DESU DEFIT Silicone Shunt
DESU MEDIKAL URUNLER VE TฤฐBBฤฐ CIHAZLAR SAN. VE TIC. A.S.
DESU External Drainage Systems
DESU MEDIKAL URUNLER VE TฤฐBBฤฐ CIHAZLAR SANAYฤฐ VE TฤฐCARET ANONฤฐM ลฤฐRKETฤฐ
JENITH-L Epidural Catheter
ZENITHT CO., LTD

