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Taiwan FDA registration 8ed1fe7d3526263259c0e89006190406

Pentax Corrective lenses (unsterilized)

TW: 賓得士 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SEIKO OPTICAL PRODUCTS CO., LTD.·Registered Oct 04, 2010 – Oct 04, 2015Cancelled
Registration details
Analysis ID
8ed1fe7d3526263259c0e89006190406
Customs Code
DHA04400929301
Company information
Manufacturer
SEIKO OPTICAL PRODUCTS CO., LTD.
Manufacturer Country
Japan
Authorized Representative
MEITATSU OPTICAL (TAIWAN) CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5844 corrective lenses
Import Information
import
Dates and status
Registration Date
Oct 04, 2010
Expiry Date
Oct 04, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for Pentax Corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ed1fe7d3526263259c0e89006190406 and manufactured by SEIKO OPTICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is MEITATSU OPTICAL (TAIWAN) CO., LTD..

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