Pure Global

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
BIODENT Denject
Analysis ID: AKL 20603023593

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BIODENT CO., LTD.

Country of Origin

Korea

Authorized Representative

TRI ANUGERAH JAYA

AR 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

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing