LUXATEMP Fluorescence - Indonesia BPOM Medical Device Registration
LUXATEMP Fluorescence is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602512705. The device is manufactured by DMG CHEMISCH-PHARMAZEUTISCHE FABRIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is THOMASONG NIRMALA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DMG CHEMISCH-PHARMAZEUTISCHE FABRIK GMBHCountry of Origin
Germany
Authorized Representative
THOMASONG NIRMALAAR Address
Jl. AM. Sangaji No. 20A
Registration Date
Feb 02, 2024
Expiry Date
Nov 24, 2028
Product Type
Prosthetic Dental Equipment
Temporary crown and bridge resin.
Non Electromedic Non Sterile
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