Taiwan FDA registration 214b5a819de2944c798bffd4564bd9ca
"Celest" surgical lamp for dental use (unsterilized)
TW: “彩樂士”手術燈牙科用(未滅菌)
Taiwan·Risk Class 1·TRILUX GMBH & CO. KG·Registered Sep 11, 2007 – Sep 11, 2012CancelledRegistration details
- Analysis ID
- 214b5a819de2944c798bffd4564bd9ca
- Customs Code
- DHA04400614602
Company information
- Manufacturer
- TRILUX GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- MEDITECHS INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Dental Surgical Light (F.4630)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4630 牙科用手術燈
- Import Information
- import
Dates and status
- Registration Date
- Sep 11, 2007
- Expiry Date
- Sep 11, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Celest" surgical lamp for dental use (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 214b5a819de2944c798bffd4564bd9ca and manufactured by TRILUX GMBH & CO. KG. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS CO., LTD..
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