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Gemini 810 + 980 Diode Laser Kit & Accessories - Indonesia BPOM Medical Device Registration

Gemini 810 + 980 Diode Laser Kit & Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222785. The device is manufactured by ALL QUALITY & SERVICES INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.

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BPOM Registered
Risk Class Kelas Resiko : C
Gemini 810 + 980 Diode Laser Kit & Accessories
Analysis ID: AKL 21603222785

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. FONDACO JAYATAMA

AR Address

Agung Podomoro Land Tower, Podomoro City Lt. 27 T1, T2, T5 Jl. Letnan Jendral Siswondo Parman Kav. 28 Kel. Tanjung Duren Selatan, Kec. Grogol Petamburan, Jakarta Barat, DKI Jakarta

Registration Date

Nov 23, 2022

Expiry Date

Sep 17, 2025

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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