HARDENING 2.0 - Indonesia BPOM Medical Device Registration
HARDENING 2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325582. The device is manufactured by QUANTEQ 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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CORAGE 2.0
Risk Classification
Product Class
Kelas : 2
Manufacturer
QUANTEQ 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
Nov 24, 2023
Expiry Date
Jun 09, 2028
Product Type
Surgical Equipment
Electrosurgical device for over-the-counter aesthetic use
Non Radiation Electromedics
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