IRE Surgical Fiber - Indonesia BPOM Medical Device Registration
IRE Surgical Fiber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325592. The device is manufactured by IRE-POLUS LTD. from Russia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRITRA PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IRE-POLUS LTD.Country of Origin
Russia
Authorized Representative
TRITRA PRIMA INDONESIAAR Address
Central Park Cikarang Blok A1 No. 02
Registration Date
Nov 24, 2023
Expiry Date
Sep 25, 2028
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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