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MEGAGEN ST Internal Fixture - Indonesia BPOM Medical Device Registration

MEGAGEN ST Internal Fixture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602520026. The device is manufactured by MEGAGEN IMPLANT CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEGAGEN IMPLANT 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 : C
MEGAGEN ST Internal Fixture
Analysis ID: AKL 20602520026

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MEGAGEN IMPLANT INDONESIA

AR Address

Capital Place Lantai 28 Unit C, Jalan Jend. Gatot Subroto Kav. 18

Registration Date

Jan 15, 2025

Expiry Date

Sep 30, 2029

Product Type

Prosthetic Dental Equipment

Endosseous dental implant

Non Electromedic Sterile

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