LnK Spinal Instrument System (2) - Indonesia BPOM Medical Device Registration
LnK Spinal Instrument System (2) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420225. The device is manufactured by L&K BIOMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is INTER RAYA.
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Risk Classification
Product Class
Kelas : 1
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
Jul 11, 2024
Expiry Date
Feb 28, 2029
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
LnK Spinal Instrument System (3)
LnK Spinal Instrument System (1)
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LDK Surgical Instruments for Prosthesis (2)
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LDK Surgical Instruments for Prosthesis (1)
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LDK Surgical Instruments for Prosthesis (3)
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LnK Spinal Instrument System (1)
L&K BIOMED CO., LTD.
LnK Spinal Instrument System (3)
L&K BIOMED CO., LTD.