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PAIN BLOCK - Indonesia BPOM Medical Device Registration

PAIN BLOCK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003022837. The device is manufactured by KOIBIG CO. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KMD INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
PAIN BLOCK
Analysis ID: AKL 21003022837

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

KOIBIG CO.

Country of Origin

Korea

Authorized Representative

PT. KMD INDONESIA

AR Address

Menara Palma lantai 7-06B, Jl. HR. Rasuna Said, Blok X2 Kav. 6

Registration Date

May 19, 2020

Expiry Date

Jan 02, 2025

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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