BIODENT Denject - Indonesia BPOM Medical Device Registration
BIODENT Denject is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603023593. The device is manufactured by BIODENT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. 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
BIODENT CO., LTD.Country of Origin
Korea
Authorized Representative
TRI ANUGERAH JAYAAR Address
Jl. Raya Pos Pengumben 34 G, RT/RW 002/005
Registration Date
Jun 30, 2020
Expiry Date
Mar 23, 2025
Product Type
Surgical Dental Equipment
Dental injecting needle.
Non Electromedic Sterile
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