Taiwan FDA registration 567980911ac1462667218140f9a60a32
"Best Der" Keman root canal center column nail (unsterilized)
TW: “百世德”克曼根管中心柱釘 (未滅菌)
Taiwan·Risk Class 1·GEBR. BRASSELER GMBH & CO. KG·Registered Sep 03, 2008 – Sep 03, 2013CancelledRegistration details
- Analysis ID
- 567980911ac1462667218140f9a60a32
- Customs Code
- DHA04400703801
Company information
- Manufacturer
- GEBR. BRASSELER GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- DENSO SCIENTIFIC CO., LTD.
Product details
- Intended Use
- Limit the scope of the first class of the medical equipment management method "Root Canal Central Column (F.3810)". Dosage =
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3810 Root canal center post
- Import Information
- import
Dates and status
- Registration Date
- Sep 03, 2008
- Expiry Date
- Sep 03, 2013
- Cancellation Date
- Jun 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Best Der" Keman root canal center column nail (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 567980911ac1462667218140f9a60a32 and manufactured by GEBR. BRASSELER GMBH & CO. KG. The authorized representative in Taiwan is DENSO SCIENTIFIC CO., LTD..
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