OPHTEIS FR Pro - Indonesia BPOM Medical Device Registration
OPHTEIS FR Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203812480. The device is manufactured by VSY BIYOTEKNOLOJI Ve IIac Sanayi Anonim Sirketi from Turkey, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BT. Encheval Putera Megatrading.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
VSY BIYOTEKNOLOJI Ve IIac Sanayi Anonim SirketiCountry of Origin
Turkey
Authorized Representative
BT. Encheval Putera MegatradingAR Address
JL PULO LENTUT NO. 10 KWS INDUSTRI PULO GADUNG
Registration Date
Jan 23, 2025
Expiry Date
May 20, 2029
Product Type
Surgical Eye Equipment
Intraocular fluid.
Non Electromedic Sterile
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