Taiwan FDA registration 3f3e7be934531e01dd6cedbc15860d7e
"Gusha" Pareki substrate
TW: "古莎" 帕樂基底材
Taiwan·Risk Class 2·Kulzer GmbH;; Kulzer SRL·Registered Mar 20, 2006 – Mar 20, 2021CancelledRegistration details
- Analysis ID
- 3f3e7be934531e01dd6cedbc15860d7e
- Customs Code
- DHA00601416801
Company information
- Manufacturer
- Kulzer GmbH;; Kulzer SRL
- Manufacturer Country
- Romania;;Germany
- Authorized Representative
- TEI JEL ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Import Information
- import
Dates and status
- Registration Date
- Mar 20, 2006
- Expiry Date
- Mar 20, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Gusha" Pareki substrate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f3e7be934531e01dd6cedbc15860d7e and manufactured by Kulzer GmbH;; Kulzer SRL. The authorized representative in Taiwan is TEI JEL ENTERPRISE CO., LTD..
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