JENITH-L Epidural Catheter - Indonesia BPOM Medical Device Registration
JENITH-L Epidural Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420381. The device is manufactured by ZENITHT CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CHAKRA JAYA 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
ZENITHT CO., LTDCountry 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
May 25, 2024
Expiry Date
Jan 17, 2029
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction catheter.
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
ZENITHT ZEUS Kyphoplasty Balloon Catheter System
ZENITHT CO., LTD.