Taiwan FDA registration e161b78e86e0d4ad0d1b3a68dc9d86b8

"Alcon" flexible intraocular lens delivery system (unsterilized)

TW: "愛爾康"可舒軟式人工水晶體輸送系統(未滅菌)

Taiwan·Risk Class 1·ALCON MANUFACTURING, LTD.·Registered Aug 30, 2007 – Aug 30, 2012Cancelled

Registration details

Analysis ID: e161b78e86e0d4ad0d1b3a68dc9d86b8
Customs Code: DHA04400611300

Company information

Manufacturer: ALCON MANUFACTURING, LTD.
Manufacturer Country: United States
Authorized Representative: ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)

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: import

Dates and status

Registration Date: Aug 30, 2007
Expiry Date: Aug 30, 2012
Cancellation Date: Apr 14, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Alcon" flexible intraocular lens delivery system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e161b78e86e0d4ad0d1b3a68dc9d86b8 and manufactured by ALCON MANUFACTURING, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).

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