CYTOPLAST PTFE Suture - Indonesia BPOM Medical Device Registration
CYTOPLAST PTFE Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022269. The device is manufactured by OSTEOGENICS BIOMEDICAL, INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FONDACO JAYATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OSTEOGENICS BIOMEDICAL, INCCountry of Origin
United States
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
Oct 10, 2024
Expiry Date
Aug 22, 2029
Product Type
Surgical Equipment
Nonabsorbable expanded polytetrafluoroethylene surgical suture.
Non Electromedic 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
3SHAPE Implant Studio
3SHAPE A/S
NEODENT Titanium Base Abutment
JJGC INDúSTRIA E COMéRCIO DE MATERIAIS DENTáRIOS SA
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
TWIN IN MOTION
MODJAW SAS
3SHAPE Lab Scanner System
3SHAPE POLAND SP. Z O. O.