Taiwan FDA registration 79004c89104c2ea01c9f1e7beac4432a
“Medipak”Dental hand instruments (Non-Sterile)
TW: “馬迪沛克”牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·MEDIPAK MANUFACTURING CORP.·Registered Sep 26, 2013 – Sep 26, 2028ActiveRegistration details
- Analysis ID
- 79004c89104c2ea01c9f1e7beac4432a
- License Form
- Ministry of Health Medical Device Import No. 013449
- Customs Code
- DHA09401344901
Company information
- Manufacturer
- MEDIPAK MANUFACTURING CORP.
- Manufacturer Country
- Pakistan
- Authorized Representative
- SUN-BRIGHT DENTAL PRODUCT 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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 26, 2013
- Expiry Date
- Sep 26, 2028
About this record
Access comprehensive regulatory information for “Medipak”Dental hand instruments (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 79004c89104c2ea01c9f1e7beac4432a and manufactured by MEDIPAK MANUFACTURING CORP.. The authorized representative in Taiwan is SUN-BRIGHT DENTAL PRODUCT CO., LTD..
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