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MICROTARGETING Guideline 4000 5.0 - Indonesia BPOM Medical Device Registration

MICROTARGETING Guideline 4000 5.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001220001. The device is manufactured by FHC, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
MICROTARGETING Guideline 4000 5.0
Analysis ID: AKL 21001220001

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

FHC, INC.

Country of Origin

United States

Authorized Representative

PT. ASIA ACTUAL INDONESIA

AR Address

PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN

Registration Date

Jan 06, 2022

Expiry Date

Apr 27, 2026

Product Type

Diagnostic Neurology Equipment

Depth electrode.

Non Radiation Electromedics

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