FOTEK Electric Surgery High Frequency Device - Indonesia BPOM Medical Device Registration
FOTEK Electric Surgery High Frequency Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603124524. The device is manufactured by PHOTOS OOO from Russia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is JEMA INDO MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHOTOS OOOCountry of Origin
Russia
Authorized Representative
JEMA INDO MANDIRIAR Address
Jl. R.S Fatmawati No.100 E, RT 001/RW 009 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selatan, DKI Jakarta - 12430
Registration Date
Aug 22, 2023
Expiry Date
Jul 26, 2026
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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