LnK Lumbar Interbody Fusion Cage System - Indonesia BPOM Medical Device Registration
LnK Lumbar Interbody Fusion Cage System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420201. The device is manufactured by L&K BIOMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INTER RAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
L&K BIOMED CO., LTD.Country of Origin
Korea
Authorized Representative
INTER RAYAAR Address
Bintaro Business Center, Jl. RC Veteran No.1-i, Pesanggrahan - Jakarta Selatan
Registration Date
Jun 03, 2024
Expiry Date
Feb 28, 2029
Product Type
Prosthetic Orthopedic Equipment
Intervertebral body fusion device
Non Electromedic Non Sterile
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LnK Spinal Instrument System (2)
LnK Spinal Instrument System (1)
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