Taiwan FDA registration e16e74cd8d9cf098b08eff8402d7336c

"Zeiss" ophthalmic laser system

TW: "蔡司"眼科雷射系統
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered May 26, 2006 – May 26, 2021Cancelled
Registration details
Analysis ID
e16e74cd8d9cf098b08eff8402d7336c
Customs Code
DHA00601451200
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.4392 後囊切除用Nd:YAG雷射
Import Information
import
Dates and status
Registration Date
May 26, 2006
Expiry Date
May 26, 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 e16e74cd8d9cf098b08eff8402d7336c 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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