Taiwan FDA registration 52e835e1bc738c12316dfd614ef97393
Covey Kitai
TW: 柯威基台
Registration details
- Analysis ID
- 52e835e1bc738c12316dfd614ef97393
- Customs Code
- DHA00602513701
Company information
- Manufacturer
- Cowellmed Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TAIWAN COWELLMEDI CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3630 Bolsters for intraosseous implants
- Import Information
- import
Dates and status
- Registration Date
- Jun 22, 2013
- Expiry Date
- Jun 22, 2028
About this record
Access comprehensive regulatory information for Covey Kitai in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52e835e1bc738c12316dfd614ef97393 and manufactured by Cowellmed Co., Ltd.. The authorized representative in Taiwan is TAIWAN COWELLMEDI CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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