Pure Global

DiaEtch - Indonesia BPOM Medical Device Registration

DiaEtch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220185. The device is manufactured by DIADENT GROUP INTERNATIONAL from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MORITA DENTAL INDO.

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
DiaEtch
Analysis ID: AKL 20602220185

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MORITA DENTAL INDO

AR Address

Ruko Roxy Trade Center Jl. KH. Hasyim Ashari No.233 K Kel.Cideng Kec.Gambir

Registration Date

Jul 30, 2022

Expiry Date

Oct 19, 2026

Product Type

Prosthetic Dental Equipment

Resin tooth bonding agent.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing