Gemini EVO 810 + 980 Diode Laser Kit & Accessories - Indonesia BPOM Medical Device Registration
Gemini EVO 810 + 980 Diode Laser Kit & Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325288. The device is manufactured by ALL QUALITY & SERVICES (AQS) INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
ALL QUALITY & SERVICES (AQS) INC.Country of Origin
United States
Authorized Representative
PT. FONDACO JAYATAMAAR 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
Oct 19, 2023
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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VITA ZAHNFABRIK H. RAUTER GMBH & CO. Medical history.

