HELIOS IV 785 Q-switched Nd:YAG Laser System - Indonesia BPOM Medical Device Registration
HELIOS IV 785 Q-switched Nd:YAG Laser System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222151. The device is manufactured by LASEROPTEK CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LASEROPTEK CO., LTD.Country of Origin
Korea
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460
Registration Date
Sep 10, 2022
Expiry Date
Oct 06, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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