Taiwan FDA registration f18a14fc2772360c9cc3c85eb921d0d3
“VDW” GUTTAFUSION Gutta percha (Non-sterile)
TW: “威帝”古特服馬來膠 (未滅菌)
Taiwan·Risk Class 1·MD·VDW GMBH·Registered Oct 16, 2013 – Oct 16, 2023ExpiredRegistration details
- Analysis ID
- f18a14fc2772360c9cc3c85eb921d0d3
- License Form
- Ministry of Health Medical Device Import No. 013502
- Customs Code
- DHA09401350205
Company information
- Manufacturer
- VDW GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yida Industrial Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3850 Male-Glue
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 16, 2013
- Expiry Date
- Oct 16, 2023
About this record
Access comprehensive regulatory information for “VDW” GUTTAFUSION Gutta percha (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 f18a14fc2772360c9cc3c85eb921d0d3 and manufactured by VDW GMBH. The authorized representative in Taiwan is Yida Industrial Co., Ltd.
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