DELPHI II - Indonesia BPOM Medical Device Registration
DELPHI II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422444. The device is manufactured by CNS MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.
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
CNS MEDICAL CO., LTD.Country of Origin
Korea
Authorized Representative
PT. FAJAR SELARAS PARTNERSAR Address
RUKAN PULOGADUNG TRADE CENTRE (PTC) BLOK 8C NOMOR 28-29
Registration Date
Oct 14, 2024
Expiry Date
Oct 27, 2028
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
AnyPlusII Pedicle Screw System-6
GS MEDICAL CO., LTD.
AnyPlusII Pedicle Screw System-3
GS MEDICAL CO., LTD.
AnyPlus II Pedicle Screw System-7
GS MEDICAL CO., LTD.
AnyPlusII Pedicle Screw System-5
GS MEDICAL CO., LTD.
AnyPlusII Pedicle Screw System-4
GS MEDICAL CO., LTD.
IRENE Locking Plate System
TIANJIN ZHENGTIAN MEDICAL INSTRUMENT CO., LTD.
AnyPlusII Pedicle Screw System-2
GS MEDICAL CO., LTD.
PYXIS 3D Titanium T-PLIF Cage (Sterile)
GS MEDICAL CO., LTD.
AnyPlusII Pedicle Screw System-1
GS MEDICAL CO., LTD.
JEIL Surgical Instrument
JEIL MEDICAL CORPORATION

