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REMED Electromagnetic Stimulator - Indonesia BPOM Medical Device Registration

REMED Electromagnetic Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003713845. The device is manufactured by REMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NEURO MEDIKA SEJAHTERA.

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BPOM Registered
Risk Class Kelas Resiko : C
REMED Electromagnetic Stimulator
Analysis ID: AKL 21003713845

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

REMED CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. NEURO MEDIKA SEJAHTERA

AR Address

JL. PENJERNIHAN I NO.38

Registration Date

Jul 11, 2023

Expiry Date

Aug 13, 2024

Product Type

Therapeutic Neurology Equipment

Implanted peripheral nerve stimulator for pain relief.

Non Radiation Electromedics

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