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"Medicel" intraocular lens guide (sterilization) - Taiwan Registration 77dd8f99eaff57a78f814761e217fa2e

Access comprehensive regulatory information for "Medicel" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77dd8f99eaff57a78f814761e217fa2e and manufactured by MEDICEL AT. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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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77dd8f99eaff57a78f814761e217fa2e
Registration Details
Taiwan FDA Registration: 77dd8f99eaff57a78f814761e217fa2e
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Device Details

"Medicel" intraocular lens guide (sterilization)
TW: โ€œ็พŽ่ฟชๅกž็ˆพโ€ ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆป…่Œ)
Risk Class 1

Registration Details

77dd8f99eaff57a78f814761e217fa2e

DHA09402254205

Company Information

Switzerland

Product Details

Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

Input;; QMS/QSD

Dates and Status

Apr 27, 2021

Apr 27, 2026