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ENRAF NONIUS Electromagnetic Therapy Stimulator - Indonesia BPOM Medical Device Registration

ENRAF NONIUS Electromagnetic Therapy Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320540. The device is manufactured by REMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MURTI INDAH SENTOSA.

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BPOM Registered
Risk Class Kelas Resiko : B
ENRAF NONIUS Electromagnetic Therapy Stimulator
Analysis ID: AKL 21403320540

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REMED CO., LTD.

Country of Origin

Korea

Authorized Representative

MURTI INDAH SENTOSA

AR Address

WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH

Registration Date

May 16, 2023

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Physical Health Equipment

Powered muscle stimulator.

Non Radiation Electromedics

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