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DiaPex Plus - Indonesia BPOM Medical Device Registration

DiaPex Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605420417. 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 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
DiaPex Plus
Analysis ID: AKL 20605420417

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

MORITA DENTAL INDO

AR Address

Jalan Supiori No. 3-3A RT 003 RW 005, Provinsi DKI Jakarta, Kota Jakarta Barat, Kec. Gambir, Kel. Cideng

Registration Date

Oct 07, 2024

Expiry Date

Oct 19, 2026

Product Type

Other Dental Equipment

Dental cement

Non Electromedic Non Sterile

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