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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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BPOM Registered
Risk Class Kelas Resiko : C
ZENITHT ZEUS Kyphoplasty Balloon Catheter System
Analysis ID: AKL 21302420188

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ZENITHT CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. CHAKRA JAYA MEDIKA

AR 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

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