JOIMAX EndoLIF Cages - Indonesia BPOM Medical Device Registration
JOIMAX EndoLIF Cages is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320958. The device is manufactured by JOIMAX GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDTEK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JOIMAX GMBHCountry of Origin
Germany
Authorized Representative
MEDTEKAR Address
Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9
Registration Date
Oct 10, 2023
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Orthopedic Equipment
Intervertebral body fusion device
Non Electromedic Non Sterile
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