Taiwan FDA registration 571f6b9fe49255e6cf09aae9b0efc021

"Zeiss" ophthalmic laser system

TW: "蔡司"眼科雷射系統
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered May 30, 2006 – May 30, 2021Cancelled
Registration details
Analysis ID
571f6b9fe49255e6cf09aae9b0efc021
Customs Code
DHA00601660504
Company information
Manufacturer Country
Germany
Authorized Representative
TAIWAN INSTRUMENT CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4390 眼科雷射裝置
Import Information
import
Dates and status
Registration Date
May 30, 2006
Expiry Date
May 30, 2021
Cancellation Date
Sep 23, 2023
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Zeiss" ophthalmic laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 571f6b9fe49255e6cf09aae9b0efc021 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG, and 4 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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