ARCIOLANE 5500 - Indonesia BPOM Medical Device Registration
ARCIOLANE 5500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203717520. The device is manufactured by ARCADOPTHA SARL. from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. UNIVERSAL STAR MULTILINK.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ARCADOPTHA SARL.Country of Origin
France
Authorized Representative
PT. UNIVERSAL STAR MULTILINKAR Address
RUKO SERENADE CENTER BLOK A/27 JL.BOULEVARD GADING SERPONG TANGERANG 15810
Registration Date
Mar 25, 2023
Expiry Date
Jul 14, 2025
Product Type
Surgical Eye Equipment
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