MORIA EVOLUTION 3E Microkeratome System - Indonesia BPOM Medical Device Registration
MORIA EVOLUTION 3E Microkeratome System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203024651. The device is manufactured by MORIA S.A. from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MORIA S.A.Country of Origin
France
Authorized Representative
PT. KATAMATA OPTOMEDIKAR Address
Komplek Ketapang Indah Blok B2 No.31 Jl. KH. Zainul Arifin Kel.Krukut, Kec.Taman Sari Jakarta Barat
Registration Date
Aug 18, 2020
Expiry Date
Dec 21, 2024
Product Type
Surgical Eye Equipment
Keratome.
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