AT TORBI 709 MP - Indonesia BPOM Medical Device Registration
AT TORBI 709 MP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202313550. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
CARL ZEISS MEDITEC AGCountry of Origin
Germany
Authorized Representative
PT. ELO KARSA UTAMAAR Address
Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.
Registration Date
Mar 18, 2022
Expiry Date
May 01, 2025
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
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