Taiwan FDA registration ed9c05dd85352035d05d2b4beb167f79

"Zeiss" ophthalmic laser system

TW: “蔡司”眼科雷射系統
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered Jan 27, 2013 – Jan 27, 2023Expired
Registration details
Analysis ID
ed9c05dd85352035d05d2b4beb167f79
Customs Code
DHA00602463203
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.4690 眼科用光凝固儀
Import Information
import
Dates and status
Registration Date
Jan 27, 2013
Expiry Date
Jan 27, 2023
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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 ed9c05dd85352035d05d2b4beb167f79 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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