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MEGAGEN N2 - Indonesia BPOM Medical Device Registration

MEGAGEN N2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605128127. The device is manufactured by MEGAGEN IMPLANT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.

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 : A
MEGAGEN N2
Analysis ID: AKL 10605128127

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. HAJU MEDICAL INDONESIA

AR Address

Gd. Graha Mampang lt. 2. Jl. Mampang Prapatan Raya no. 100 Duren Tiga Pancoran

Registration Date

Dec 23, 2021

Expiry Date

Oct 25, 2026

Product Type

Other Dental Equipment

Dental operative unit and accessories.

Non Radiation Electromedics

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