VISALIS S500 - Indonesia BPOM Medical Device Registration
VISALIS S500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203413652. The device is manufactured by CARL ZEISS MEDITEC AG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARL ZEISS MEDITEC AG.Country of Origin
Germany
Authorized Representative
PT. ELO KARSA UTAMAAR Address
Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.
Registration Date
Feb 06, 2023
Expiry Date
May 01, 2025
Product Type
Surgical Eye Equipment
Phacofragmentation system.
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