SONOCARE Dual Frequency Ultrasound - Indonesia BPOM Medical Device Registration
SONOCARE Dual Frequency Ultrasound is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420286. The device is manufactured by NEWPONG CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEWPONG 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
Feb 02, 2024
Expiry Date
Nov 08, 2028
Product Type
Surgical Equipment
Focused ultrasound stimulator system for aesthetic use
Non Radiation Electromedics
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