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CROME™ HF CRT-D MRI SureScan™ - Indonesia BPOM Medical Device Registration

CROME™ HF CRT-D MRI SureScan™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503220015. The device is manufactured by MEDTRONIC EUROPE S.A.R.L from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. 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
CROME™ HF CRT-D MRI SureScan™
Analysis ID: AKL 30503220015

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Switzerland

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Jan 18, 2022

Expiry Date

Jan 13, 2026

Product Type

Prosthetic Cardiology Equipment

Automatic Implantable Cardioverter Defibrillator With Cardiac Resynchronization (Crt-D)

Non Radiation Electromedics

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