Taiwan FDA registration e8d3849c48623cebbf65f3a02e0f5d99
“DHEF” Matrix Retainer (Non-Sterile)
TW: “奇祁”基質保留器 (未滅菌)
Taiwan·Risk Class 1·MD·MEDIPAK MANUFACTURING CORP.·Registered Aug 14, 2019 – Aug 14, 2024ExpiredRegistration details
- Analysis ID
- e8d3849c48623cebbf65f3a02e0f5d99
- License Form
- Ministry of Health Medical Device Import No. 020751
- Customs Code
- DHA09402075104
Company information
- Manufacturer
- MEDIPAK MANUFACTURING CORP.
- Manufacturer Country
- Pakistan
- Authorized Representative
- DHEF INC.
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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 14, 2019
- Expiry Date
- Aug 14, 2024
About this record
Access comprehensive regulatory information for “DHEF” Matrix Retainer (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 e8d3849c48623cebbf65f3a02e0f5d99 and manufactured by MEDIPAK MANUFACTURING CORP.. The authorized representative in Taiwan is DHEF INC..
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