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MINATO KINETIZER - Indonesia BPOM Medical Device Registration

MINATO KINETIZER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003320161. The device is manufactured by MINATO MEDICAL SCIENCE CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.

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BPOM Registered
Risk Class Kelas Resiko : C
MINATO KINETIZER
Analysis ID: AKL 21003320161

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Sep 05, 2023

Expiry Date

Jan 16, 2028

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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