Taiwan FDA registration 3f7130b22a484eb6785d0b52a291d0d6
"HDI" GingiCord Retraction cord (Non-Sterile)
TW: "艾取德" 金吉可排齦線(未滅菌)
Taiwan·Risk Class 1·MD·HDI INC.·Registered Jan 25, 2018 – Jan 25, 2028ActiveRegistration details
- Analysis ID
- 3f7130b22a484eb6785d0b52a291d0d6
- License Form
- Ministry of Health Medical Device Import No. 018761
- Customs Code
- DHA09401876102
Company information
- Manufacturer
- HDI INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MNM BIOTECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F0001 Gingival drain line
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 25, 2018
- Expiry Date
- Jan 25, 2028
About this record
Access comprehensive regulatory information for "HDI" GingiCord Retraction cord (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 3f7130b22a484eb6785d0b52a291d0d6 and manufactured by HDI INC.. The authorized representative in Taiwan is MNM BIOTECHNOLOGY CO., LTD.
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