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MODULO PLUS Electrotherapy - Indonesia BPOM Medical Device Registration

MODULO PLUS Electrotherapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220020. The device is manufactured by FISIOLINE S.R.L [REGISTER] from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HARLISA TRUE AWARD.

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BPOM Registered
Risk Class Kelas Resiko : B
MODULO PLUS Electrotherapy
Analysis ID: AKL 21403220020

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

HARLISA TRUE AWARD

AR Address

Jalan Sriti Blok HH-15, Perumahan Sedati Permai

Registration Date

Jul 29, 2024

Expiry Date

Feb 13, 2027

Product Type

Therapeutic Physical Health Equipment

Powered muscle stimulator.

Non Radiation Electromedics

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