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VITATRON Q50 D MRI SureScan™ - Indonesia BPOM Medical Device Registration

VITATRON Q50 D MRI SureScan™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503816497. The device is manufactured by MEDTRONIC SINGAPORE OPERATIONS PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MEDTRONIC 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 : D
VITATRON Q50 D MRI SureScan™
Analysis ID: AKL 30503816497

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Singapore

Authorized Representative

MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Mar 29, 2024

Expiry Date

Feb 07, 2028

Product Type

Prosthetic Cardiology Equipment

Implantable pacemaker pulse generator.

Non Radiation Electromedics

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