FEMTO LDV Procedure Packs - Indonesia BPOM Medical Device Registration
FEMTO LDV Procedure Packs is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203813815. The device is manufactured by SIE AG, SURGICAL INSTRUMENT ENGINEERING from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIE AG, SURGICAL INSTRUMENT ENGINEERINGCountry of Origin
Switzerland
Authorized Representative
PT. TRIASTRI MEDITAMAAR Address
GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11
Registration Date
Jun 16, 2021
Expiry Date
Jan 10, 2024
Product Type
Surgical Eye Equipment
Ophthalmic laser.
Non Electromedic Sterile
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