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DiaPaste - Indonesia BPOM Medical Device Registration

DiaPaste is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220164. The device is manufactured by DIADENT GROUP INTERNATIONAL from Korea, and is classified as Risk Class Kelas Resiko : C. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
DiaPaste
Analysis ID: AKL 20602220164

Risk Classification

Kelas Resiko : C

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

Jun 29, 2022

Expiry Date

Oct 19, 2026

Product Type

Prosthetic Dental Equipment

Root canal filling resin

Non Electromedic Non Sterile

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