Taiwan FDA registration e53d77dddb493631a39629820a6df71d
“Kereden” temporary gingival retraction (Non-sterile)
TW: “克拉登” 暫時性排齦膏組 (未滅菌)
Taiwan·Risk Class 1·MD·KEREDEN CO. LTD.·Registered Jun 18, 2019 – Jun 18, 2024ExpiredRegistration details
- Analysis ID
- e53d77dddb493631a39629820a6df71d
- License Form
- Ministry of Health Medical Device Import No. 020565
- Customs Code
- DHA09402056507
Company information
- Manufacturer
- KEREDEN CO. LTD.
- Manufacturer Country
- France
- Authorized Representative
- LA FU INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F0001 Gingival drain line
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 18, 2019
- Expiry Date
- Jun 18, 2024
About this record
Access comprehensive regulatory information for “Kereden” temporary gingival retraction (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 e53d77dddb493631a39629820a6df71d and manufactured by KEREDEN CO. LTD.. The authorized representative in Taiwan is LA FU INDUSTRIAL CO., LTD..
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