Taiwan FDA registration 44e88df45413125f26cbfefd461f564e
“Trilux” Madidrant CSS Intensive (Non-Sterile)
TW: “崔勒斯”美帝綸德吊塔系統 (未滅菌)
Taiwan·Risk Class 1·MD·TRILUX MEDICAL GMBH & CO. KG·Registered Dec 24, 2014 – Dec 24, 2019CancelledRegistration details
- Analysis ID
- 44e88df45413125f26cbfefd461f564e
- License Form
- Ministry of Health Medical Device Import No. 014776
- Customs Code
- DHA09401477608
Company information
- Manufacturer
- TRILUX MEDICAL GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- T-SUN INTERNATIONAL CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4960 Electric or pneumatic surgical tables, chairs and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 24, 2014
- Expiry Date
- Dec 24, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Trilux” Madidrant CSS Intensive (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 44e88df45413125f26cbfefd461f564e and manufactured by TRILUX MEDICAL GMBH & CO. KG. The authorized representative in Taiwan is T-SUN INTERNATIONAL CO., LTD..
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