Taiwan FDA registration 73a2760a8a9105692857778d67a531f6

"Bausch & Len" IOL Guide (Sterilization)

TW: “博士倫”人工水晶體導引器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·MEDICEL AT·Registered Dec 26, 2013 – Dec 26, 2018Cancelled
Registration details
Analysis ID
73a2760a8a9105692857778d67a531f6
Customs Code
DHA09401372805
Company information
Manufacturer
MEDICEL AT
Manufacturer Country
Switzerland
Authorized Representative
BAUSCH & LOMB TAIWAN LIMITED
Product details
Intended Use
Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4300 Artificial crystal body inducer
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Dec 26, 2013
Expiry Date
Dec 26, 2018
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Bausch & Len" IOL 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 73a2760a8a9105692857778d67a531f6 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 BAUSCH & LOMB INC., and 2 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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