LUMEX LIFE - Indonesia BPOM Medical Device Registration
LUMEX LIFE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605120905. The device is manufactured by VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FONDACO JAYATAMA.
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VITA LUMEX
Risk Classification
Product Class
Kelas : 2
Manufacturer
VITA ZAHNFABRIK H. RAUTER GMBH & CO. KGCountry of Origin
Germany
Authorized Representative
FONDACO JAYATAMAAR Address
Agung Podomoro Land Tower, Podomoro City Lt. 27 T1, T2, T5 Jl. Letnan Jendral Siswondo Parman Kav. 28 Kel. Tanjung Duren Selatan, Kec. Grogol Petamburan, Jakarta Barat, DKI Jakarta
Registration Date
Feb 18, 2021
Expiry Date
Sep 09, 2025
Product Type
Other Dental Equipment
Porcelain powder for clinical use.
Non Electromedic Non Sterile
NEODENT Prosthetic Components in Titanium
JJGC INDúSTRIA E COMéRCIO DE MATERIAIS DENTáRIOS SA
VITA YZ T COLORING LIQUID
VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG
NEODENT Titanium Base Abutment
JJGC INDúSTRIA E COMéRCIO DE MATERIAIS DENTáRIOS SA
3SHAPE Implant Studio
3SHAPE A/S
EXOCAD Exoplan
EXOCAD GMBH
NEODENT Rotary Instruments
JJGC INDúSTRIA E COMéRCIO DE MATERIAIS DENTáRIOS SA
NEODENT Scanbody
JJGC INDUSTRIA E COMÉRCIO DE MATERIAIS DENTÁRIAS S.A-NEODENT
CURAPROX Travel Set Ortho
CURAPLAST AT
3SHAPE Lab Scanner System
3SHAPE POLAND SP. Z O. O.
TWIN IN MOTION
MODJAW SAS