Taiwan FDA registration 7f25e378c0ac95fdbc73dca21bffd315
3M ESPE Filtek Bulk Fill Flowable Restorative
TW: 3M菲特波克流動性補牙材
Taiwan·Risk Class 2·MD·3M ESPE DENTAL PRODUCTS·Registered May 07, 2018 – May 07, 2028ActiveRegistration details
- Analysis ID
- 7f25e378c0ac95fdbc73dca21bffd315
- License Form
- Ministry of Health Medical Device Import No. 031062
- Customs Code
- DHA05603106201
Company information
- Manufacturer
- 3M ESPE DENTAL PRODUCTS
- Manufacturer Country
- United States
- Authorized Representative
- 3M TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 07, 2018
- Expiry Date
- May 07, 2028
About this record
Access comprehensive regulatory information for 3M ESPE Filtek Bulk Fill Flowable Restorative in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f25e378c0ac95fdbc73dca21bffd315 and manufactured by 3M ESPE DENTAL PRODUCTS. The authorized representative in Taiwan is 3M TAIWAN LTD..
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