MENICON Rose K2 - Indonesia BPOM Medical Device Registration
MENICON Rose K2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420112. The device is manufactured by MENICON LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIUMPHANT MANDARIN OPTO-MEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MENICON LTD.Country of Origin
United Kingdom
Authorized Representative
PT. TRIUMPHANT MANDARIN OPTO-MEDICAR Address
Jl. Senen Raya No. 135 Ruko Atrium Blok C No. 15 Jakarta Pusat 10410 Tlp : 021-3515478, 3516018 Fax : 021-3511606
Registration Date
Mar 05, 2024
Expiry Date
Dec 31, 2027
Product Type
Therapeutic Eye Equipment
Rigid gas permeable contact lens for daily wear only.
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