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MEDTRONIC Dual Chamber Temporary External Pacemaker - Indonesia BPOM Medical Device Registration

MEDTRONIC Dual Chamber Temporary External Pacemaker is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503413100. The device is manufactured by PLEXUS MANUFACTURING SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
MEDTRONIC Dual Chamber Temporary External Pacemaker
Analysis ID: AKL 30503413100

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Malaysia

Authorized Representative

PT. 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

Oct 10, 2024

Expiry Date

Feb 20, 2029

Product Type

Prosthetic Cardiology Equipment

External pacemaker pulse generator.

Non Radiation Electromedics

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