Taiwan FDA registration be7aeb11b2f0a4296df1d6c283b83a8b
"Manny" root canal (unextinguished)
TW: "曼尼" 根管銼(未滅菌)
Taiwan·Risk Class 1·MANI,INC.·Registered Apr 27, 2006 – Apr 27, 2011CancelledRegistration details
- Analysis ID
- be7aeb11b2f0a4296df1d6c283b83a8b
- Customs Code
- DHA04400425405
Company information
- Manufacturer
- MANI,INC.
- Manufacturer Country
- Japan
- Authorized Representative
- APOZA ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- Apr 27, 2006
- Expiry Date
- Apr 27, 2011
- Cancellation Date
- Jul 07, 2011
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Manny" root canal (unextinguished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be7aeb11b2f0a4296df1d6c283b83a8b and manufactured by MANI,INC.. The authorized representative in Taiwan is APOZA ENTERPRISE 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