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DIAMOND Corrective Spectacle Lens(Non-Sterile) - Taiwan Registration 9d4398e92ad812097963fbb608cf5136

Access comprehensive regulatory information for DIAMOND Corrective Spectacle Lens(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d4398e92ad812097963fbb608cf5136 and manufactured by Hong Kong Optical Lens Phils. Laboratory Inc. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

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9d4398e92ad812097963fbb608cf5136
Registration Details
Taiwan FDA Registration: 9d4398e92ad812097963fbb608cf5136
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Device Details

DIAMOND Corrective Spectacle Lens(Non-Sterile)
TW: ๆ™ถ้‘ฝ ็Ÿฏๆญฃ้ก็‰‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9d4398e92ad812097963fbb608cf5136

Ministry of Health Medical Device Import No. 023046

DHA09402304601

Company Information

Product Details

Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M5844 corrective lenses

Imported from abroad

Dates and Status

Feb 15, 2023

Feb 15, 2028