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MEDTRONIC Single Chamber Temporary External Pacemaker 53401 - Indonesia BPOM Medical Device Registration

MEDTRONIC Single Chamber Temporary External Pacemaker 53401 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503719274. 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 Single Chamber Temporary External Pacemaker 53401
Analysis ID: AKL 30503719274

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

Registration Date

May 20, 2022

Expiry Date

Feb 16, 2027

Product Type

Prosthetic Cardiology Equipment

External pacemaker pulse generator.

Non Radiation Electromedics

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