MASTER-DENT Light Cure Cavity Liner - Indonesia BPOM Medical Device Registration
MASTER-DENT Light Cure Cavity Liner is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602520052. The device is manufactured by DENTONICS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRI ANUGERAH JAYA.
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 : 2
Manufacturer
DENTONICS, INC.Country of Origin
United States
Authorized Representative
TRI ANUGERAH JAYAAR Address
Jl. Raya Pos Pengumben 34 G
Registration Date
Feb 10, 2025
Expiry Date
Nov 01, 2029
Product Type
Prosthetic Dental Equipment
Calcium hydroxide cavity liner.
Non Electromedic Non Sterile
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