Taiwan FDA registration bc83530f8e52654aecccefb5b2d692e7
"Kejie" Rininbayer backbone
TW: "可捷"瑞寧拜爾支台齒
Taiwan·KJ MEDITECH·Registered Jun 16, 2004 – Jun 16, 2009CancelledRegistration details
- Analysis ID
- bc83530f8e52654aecccefb5b2d692e7
- Customs Code
- DHA00601072306
Company information
- Manufacturer
- KJ MEDITECH
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- New Tooth Technology Co., Ltd
Product details
- Product Type (Level 1)
- F Dentistry
- Import Information
- import
Dates and status
- Registration Date
- Jun 16, 2004
- Expiry Date
- Jun 16, 2009
- Cancellation Date
- Oct 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kejie" Rininbayer backbone in Taiwan's medical device market through Pure Global AI's free database. is registered under number bc83530f8e52654aecccefb5b2d692e7 and manufactured by KJ MEDITECH. The authorized representative in Taiwan is New Tooth Technology 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.
Free DatabasePowered by Pure Global AI89,000+ Devices