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"Medis" intraocular lens guide (sterilization) - Taiwan Registration 102cd2075211d62520d41007a8d22a72

Access comprehensive regulatory information for "Medis" 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 102cd2075211d62520d41007a8d22a72 and manufactured by MEDICEL AT. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDICEL AT, and 1 recent registrations in the same category. 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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102cd2075211d62520d41007a8d22a72
Registration Details
Taiwan FDA Registration: 102cd2075211d62520d41007a8d22a72
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Device Details

"Medis" intraocular lens guide (sterilization)
TW: "้บฅ่ฟชๆ–ฏ" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆป…่Œ)
Risk Class 1

Registration Details

102cd2075211d62520d41007a8d22a72

DHA09401764508

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Mar 24, 2017

Mar 24, 2027

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