CUVIS-Spine - Indonesia BPOM Medical Device Registration
CUVIS-Spine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002320133. The device is manufactured by CUREXO INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SKBIO NUSA MEDICA.
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
CUREXO INC.Country of Origin
Korea
Authorized Representative
SKBIO NUSA MEDICAAR Address
KOMPLEK WIJAYA GRAHA PURI BLOK G NO. 17 LT. 3 JL. WIJAYA II, KEL. PULO KEC. KEBAYORAN BARU JAKARTA SELATAN
Registration Date
May 10, 2023
Expiry Date
Dec 21, 2027
Product Type
Surgical Neurology Equipment
Stereotaxic instrument.
Non Radiation Electromedics
Kyphoplasty Balloon System (KYBS)
OK MEDINET KOREA CO., LTD.
OK MEDINET Percutaneous Vertebroplasty Puncture Needle
OK MEDINET KOREA CO., LTD.
RF-Curer Electrosurgical System Electrode
OK MEDINET KOREA CO., LTD.
PERFECT-C
SEOHANCARE CO., LTD.
ESSORB Cog Polydioxanone Suture
PINE BM CO., LTD.
ESSORB Polydioxanone Suture
PINE BM CO., LTD.
HKT Retractor
HANKIL TECH MEDICAL CO., LTD.
HKT Probe
HANKIL TECH MEDICAL CO., LTD.
TECHCORD Instrument Set
TECHCORD CO., LTD.
TECHCORD ENDOSCOPIC DILATOR SHEATH
TECHCORD CO., LTD.

