FEMTO Z8 NEO - Indonesia BPOM Medical Device Registration
FEMTO Z8 NEO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203220164. 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
JL. INDUSTRI NO.9-11 GUNUNG SAHARI UTARA,
Registration Date
Jun 16, 2023
Expiry Date
May 08, 2028
Product Type
Surgical Eye Equipment
Ophthalmic laser.
Non Radiation Electromedics
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