Taiwan FDA registration 059bbae45c36e38485316d126660dff9

"Zeiss" ophthalmic laser system

TW: "蔡司"眼科雷射系統
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered May 24, 2006 – May 24, 2011Cancelled
Registration details
Analysis ID
059bbae45c36e38485316d126660dff9
Customs Code
DHA00601450707
Company information
Manufacturer Country
Germany
Authorized Representative
Taiwan Instrument Company 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 24, 2006
Expiry Date
May 24, 2011
Cancellation Date
Nov 16, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 059bbae45c36e38485316d126660dff9 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is Taiwan Instrument Company 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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