SKYPULSE® - Indonesia BPOM Medical Device Registration
SKYPULSE® is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603024584. The device is manufactured by PHOTONA D.O.O. from Slovenia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ADMIRAL BLESENSA IMMORTAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHOTONA D.O.O.Country of Origin
Slovenia
Authorized Representative
ADMIRAL BLESENSA IMMORTALAR Address
Ruko Graha Handaya unit H Jl. Raya Pejuangan Kav. 12A, Kebon Jeruk, Kota Jakarta Barat, Kode Pos 11530
Registration Date
Sep 26, 2023
Expiry Date
Jul 27, 2028
Product Type
Surgical Dental Equipment
Dental electrosurgical unit and accessories.
Non Radiation Electromedics
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