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SwiftMR A22-OP - Indonesia BPOM Medical Device Registration

SwiftMR A22-OP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321025. The device is manufactured by AIRS MEDICAL INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL 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
SwiftMR A22-OP
Analysis ID: AKL 21501321025

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

AIRS MEDICAL INC.

Country of Origin

Korea

Authorized Representative

PT. ASIA ACTUAL INDONESIA

AR Address

PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN

Registration Date

Dec 13, 2023

Expiry Date

Apr 28, 2028

Product Type

Diagnostic Radiology Equipment

Medical image management and processing system.

Non Radiation Electromedics

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