ESSILOR Refraction - Indonesia BPOM Medical Device Registration
ESSILOR Refraction is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102128137. The device is manufactured by YURATEK ELEKTRONIK VE TIBBI CIHAZLAR LTD., STI. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OPTICAL PARTNERS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
YURATEK ELEKTRONIK VE TIBBI CIHAZLAR LTD., STI.Country of Origin
Turkey
Authorized Representative
PT. OPTICAL PARTNERS INDONESIAAR Address
JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN
Registration Date
Dec 23, 2021
Expiry Date
Aug 31, 2025
Product Type
Clinical Laboratory Equipment
Refractometer for clinical use. (Electrically Operated)
Non Radiation Electromedics
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