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FOHOWAY Photon Device Pro (PDP) - Indonesia BPOM Medical Device Registration

FOHOWAY Photon Device Pro (PDP) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420305. The device is manufactured by GUANGZHOU AUKEWEL ELECTRONIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOHERB INTERNATIONAL TRADING.

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BPOM Registered
Risk Class Kelas Resiko : B
FOHOWAY Photon Device Pro (PDP)
Analysis ID: AKL 21403420305

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FOHERB INTERNATIONAL TRADING

AR Address

KEM TOWER LANTAI 9, JALAN LANDASAN PACU BARAT NOMOR 2 BLOK B-10, RW 10, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Kemayoran, Kel. Kuningan Timur

Registration Date

Aug 04, 2024

Expiry Date

Aug 01, 2027

Product Type

Therapeutic Physical Health Equipment

Ultrasound and muscle stimulator for use in applying therapeutic deep heat for selected medical conditions

Non Radiation Electromedics

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