OK Coablation - Indonesia BPOM Medical Device Registration
OK Coablation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323800. The device is manufactured by OK MEDINET KOREA CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SKBIO NUSA MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OK MEDINET KOREA CO., LTD.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
Apr 20, 2023
Expiry Date
Dec 04, 2027
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
Kyphoplasty Balloon System (KYBS)
OK MEDINET Percutaneous Vertebroplasty Puncture Needle
RF-Curer Electrosurgical System Electrode
RF-Curer Electrosurgical System Electrode
OK MEDINET Percutaneous Vertebroplasty Puncture Needle
KYBS (Kyphoplasty Balloon System) Osteo Toolkit Set
KYBS (Kyphoplasty Balloon System) Dilator Balloon
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.
CUVIS-Spine
CUREXO INC.