RODENSTOCK Refraction Unit - Indonesia BPOM Medical Device Registration
RODENSTOCK Refraction Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203412381. The device is manufactured by MDT. from Poland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MDT.Country of Origin
Poland
Authorized Representative
PT. EAST RAYA LESTARIAR Address
Jl. Rawa Kepiting No. 4, Kawasan Industri Pulogadung
Registration Date
Oct 16, 2023
Expiry Date
Dec 31, 2025
Product Type
Surgical Eye Equipment
Ophthalmic instrument table.
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