VISIONIX Handheld Auto Refract Keratometer Retinomax K+Screen - Indonesia BPOM Medical Device Registration
VISIONIX Handheld Auto Refract Keratometer Retinomax K+Screen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201320334. The device is manufactured by TOHOKU RIGHT MFG CO.,LTD OSATO FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRIUMPHANT MANDARIN OPTO-MEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TOHOKU RIGHT MFG CO.,LTD OSATO FACTORYCountry of Origin
Japan
Authorized Representative
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
Jun 23, 2023
Expiry Date
Dec 31, 2025
Product Type
Diagnostic Eye Equipment
AC-powered slitlamp biomicroscope.
Non Electromedic Non Sterile
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