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REMEDI Portable X-Ray - Indonesia BPOM Medical Device Registration

REMEDI Portable X-Ray is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321020. The device is manufactured by REMEDI CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NATIONAL HARMONY OF INDONESIAN TECHNOLOGY.

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
REMEDI Portable X-Ray
Analysis ID: AKL 21501321020

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

REMEDI CO., LTD.

Country of Origin

Korea

AR Address

Ruko Rich Palace, No.36-40 Blok D5, Jl. Meruya Ilir, Srengseng, Kembangan, Jakarta Barat

Registration Date

Jun 11, 2023

Expiry Date

Mar 31, 2027

Product Type

Diagnostic Radiology Equipment

Mobile x-ray system.

Electromedic Radiation

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