CATARHEX 3 Phacoemulsifiication System - Indonesia BPOM Medical Device Registration
CATARHEX 3 Phacoemulsifiication System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203912112. The device is manufactured by OERTLI INSTRUMENTE AG. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OERTLI INSTRUMENTE AG.Country of Origin
Switzerland
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
Jul 06, 2023
Expiry Date
Dec 05, 2027
Product Type
Surgical Eye Equipment
Phacofragmentation system.
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