KETTENBACH Identium Light - Indonesia BPOM Medical Device Registration
KETTENBACH Identium Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602812254. The device is manufactured by KETTENBACH GMBH & CO. Medical history. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KETTENBACH GMBH & CO. Medical history.Country of Origin
Germany
Authorized Representative
PT. FONDACO JAYATAMAAR Address
APL Tower Podomoro City Lantai 27 T1, T2, T5, Jln Letjen S. Parman Kavling 28
Registration Date
Nov 12, 2024
Expiry Date
Dec 18, 2025
Product Type
Prosthetic Dental Equipment
Impression material.
Non Electromedic Non Sterile
PANASIL PUTTY
PANASIL Initial Contact X-Light
KETTENBACH Identium Medium
KETTENBACH PANASIL Monophase Medium
KETTENBACH PANASIL Contact Two in One Light
PANASIL Contact Plus X-Light
KETTENBACH Futar D
VITA YZ
VITA ZAHNFABRIK H. RAUTER GMBH & CO. Medical history
NEODENT Rotary Instruments in Stainless Steel
JJGC INDúSTRIA E COMéRCIO DE MATERIAIS DENTáRIOS SA
NEODENT Manual Drivers and Connections
JJGC INDUSTRIA E COMÉRCIO DE MATERIAIS DENTÁRIAS S.A-NEODENT
VITA VMK Master Powders
VITA ZAHNFABRIK H. RAUTER GMBH & CO. Medical history.
VITA VM9 Powders
VITA ZAHNFABRIK H. RAUTER GMBH & CO., KG.
ENAMIC LIFE
VITA ZAHNFABRIK H. RAUTER GMBH & CO. Medical history
VITA AKZENT Plus Powders
VITA ZAHNFABRIK H. RAUTER GMBH & CO., KG.
VITA VM11 Powders
VITA ZAHNFABRIK H. RAUTER GMBH & CO., KG.
NEODENT Surgical Kit Case
JJGC INDUSTRIA E COMÉRCIO DE MATERIAIS DENTÁRIAS S.A-NEODENT
VITA SUPRINITY PC
VITA ZAHNFABRIK H. RAUTER GMBH & CO. Medical history.