Taiwan FDA registration 301fbaddd0a9a638152d5a5c8aa5923c
Argon-pigment laser device
TW: 氬-色素雷射裝置
Registration details
- Analysis ID
- 301fbaddd0a9a638152d5a5c8aa5923c
- Customs Code
- DHA00600376100
Company information
- Manufacturer
- COOPERVISION, INC., LASER DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- German-English Co., Ltd
Product details
- Product Type (Level 1)
- 2199 Other medical laser devices
- Import Information
- import
Dates and status
- Registration Date
- Jul 30, 1985
- Expiry Date
- Jul 30, 1990
- Cancellation Date
- Dec 13, 2004
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Argon-pigment laser device in Taiwan's medical device market through Pure Global AI's free database. is registered under number 301fbaddd0a9a638152d5a5c8aa5923c and manufactured by COOPERVISION, INC., LASER DIVISION. The authorized representative in Taiwan is German-English Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices