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"Artinis" Transilluminator (Non-Sterile) - Taiwan Registration b33dad573b5a2188e1962500a7d8e8a8

Access comprehensive regulatory information for "Artinis" Transilluminator (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 b33dad573b5a2188e1962500a7d8e8a8 and manufactured by ARTINIS MEDICAL SYSTEMS. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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b33dad573b5a2188e1962500a7d8e8a8
Registration Details
Taiwan FDA Registration: b33dad573b5a2188e1962500a7d8e8a8
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Device Details

"Artinis" Transilluminator (Non-Sterile)
TW: "้˜ฟๅพทๅฐผๆ–ฏ" ่ก€็ฎก้€็…งๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b33dad573b5a2188e1962500a7d8e8a8

Ministry of Health Medical Device Import No. 017634

DHA09401763403

Company Information

Netherlands

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".

M Ophthalmic devices

M1945 transillumination

Imported from abroad

Dates and Status

Mar 22, 2017

Mar 22, 2022