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“OCULAR” Diagnostic condensing lens (Non-Sterile) - Taiwan Registration 9c146e44d29ab90f17c1e33892b4045d

Access comprehensive regulatory information for “OCULAR” Diagnostic condensing 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 9c146e44d29ab90f17c1e33892b4045d and manufactured by OCULAR INSTRUMENTS, INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT 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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9c146e44d29ab90f17c1e33892b4045d
Registration Details
Taiwan FDA Registration: 9c146e44d29ab90f17c1e33892b4045d
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Device Details

“OCULAR” Diagnostic condensing lens (Non-Sterile)
TW: “歐可爾”診斷用鏡片 ( 未滅菌)
Risk Class 1
MD

Registration Details

9c146e44d29ab90f17c1e33892b4045d

Ministry of Health Medical Device Import No. 016785

DHA09401678506

Company Information

United States

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Diagnostic Condensing Lenses (M.1380)".

M Ophthalmic devices

M1380 Diagnostic Condensing Lens

Imported from abroad

Dates and Status

Jul 15, 2016

Jul 15, 2026