ENDO Titanium Trauma Implants Screw - Indonesia BPOM Medical Device Registration
ENDO Titanium Trauma Implants Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302816945. 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 ENDO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
ENDO INDONESIAAR Address
Jl. Raya Menganti 14
Registration Date
May 25, 2021
Expiry Date
May 24, 2024
Product Type
Prosthetic Orthopedic Equipment
Smooth or threaded metallic bone fixation fastener.
Non Electromedic Non Sterile
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