KANGLI Spinal Fixation - Indonesia BPOM Medical Device Registration
KANGLI Spinal Fixation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302220249. The device is manufactured by SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JAVA ALMEDA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. JAVA ALMEDA MANDIRIAR Address
PERUMAHAN GUNUNG SARI INDAH BLOK RR NO.4 SURABAYA 60223
Registration Date
Jun 13, 2022
Expiry Date
Apr 12, 2026
Product Type
Prosthetic Orthopedic Equipment
Pedicle screw spinal system
Non Electromedic Non Sterile
ENDO Trauma Implants Instruments
PROTECT - Screw Driver
ENDO Metal Anatomical Bone Plate
ENDO Metal Locking Plate System
ENDO Titanium Trauma Implants Screw
PROTECT Mini Screw
KANGLI METAL LOCKING PLATE SYSTEM
KANGLI METAL BONE SCREW
ENDO Trauma Implants Plates
KANGLI Metal Bone Screw
KANGLI METAL LOCKING PLATE SYSTEM
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.
KANGLI METAL BONE SCREW
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.
KANGLI Metal Bone Screw
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.
KANGLI Metal Locking Plate System
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.
KANGLI Metal locking Screw
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.

