LUXAPOST - Indonesia BPOM Medical Device Registration
LUXAPOST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602911878. The device is manufactured by DMG CHEMISCH-PHARMAZEUTISCHE FAVRIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. THOMASONG NIRMALA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
DMG CHEMISCH-PHARMAZEUTISCHE FAVRIK GMBHCountry of Origin
Germany
Authorized Representative
PT. THOMASONG NIRMALAAR Address
Jl. AM. Sangaji No. 20A
Registration Date
Feb 02, 2024
Expiry Date
Dec 31, 2026
Product Type
Prosthetic Dental Equipment
Root canal post.
Non Electromedic Non Sterile
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