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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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BPOM Registered
Risk Class Kelas Resiko : B
VISIONIX Handheld Auto Refract Keratometer Retinomax K+Screen
Analysis ID: AKL 21201320334

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

TRIUMPHANT MANDARIN OPTO-MEDIC

AR 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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