FEMTO LDV Artificial Anterior Chamber (AAC) - Indonesia BPOM Medical Device Registration
FEMTO LDV Artificial Anterior Chamber (AAC) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203918276. The device is manufactured by SIE AG, SURGICAL INSTRUMENT ENGINEERING from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SIE AG, SURGICAL INSTRUMENT ENGINEERINGCountry of Origin
Switzerland
Authorized Representative
TRIASTRI MEDITAMAAR Address
JL. INDUSTRI NO.9-11 GUNUNG SAHARI UTARA,
Registration Date
Oct 10, 2023
Expiry Date
May 08, 2028
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
Non Electromedic Non Sterile
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