NEODENT Scanbody - Indonesia BPOM Medical Device Registration
NEODENT Scanbody is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602420474. The device is manufactured by JJGC INDUSTRIA E COMÉRCIO DE MATERIAIS DENTÁRIAS S.A-NEODENT from Brazil, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FONDACO JAYATAMA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 1
Country of Origin
Brazil
Authorized Representative
FONDACO JAYATAMAAR Address
APL Tower Podomoro City Lantai 27 T1, T2, T5, Jln Letjen S. Parman Kavling 28
Registration Date
Dec 16, 2024
Expiry Date
Mar 14, 2029
Product Type
Prosthetic Dental Equipment
Endosseous dental implant accessories.
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
CURAPROX Travel Set Ortho
CURAPLAST AT
3SHAPE Lab Scanner System
3SHAPE POLAND SP. Z O. O.
TWIN IN MOTION
MODJAW SAS
CYTOPLAST PTFE Suture
OSTEOGENICS BIOMEDICAL, INC

