Taiwan FDA registration fce09b32338a949d1a0c7545d15990b5
"Nexobio" Retraction Paste (Non-sterile)
TW: "奈梭拜耳" 排齦膏 (未滅菌)
Taiwan·Risk Class 1·MD·NEXOBIO Co., Ltd.·Registered Jun 21, 2017 – Jun 21, 2027ActiveRegistration details
- Analysis ID
- fce09b32338a949d1a0c7545d15990b5
- License Form
- Ministry of Health Medical Device Import No. 018001
- Customs Code
- DHA09401800108
Company information
- Manufacturer
- NEXOBIO Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HSIN HUI MEDICAL 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
- Jun 21, 2017
- Expiry Date
- Jun 21, 2027
About this record
Access comprehensive regulatory information for "Nexobio" Retraction Paste (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 fce09b32338a949d1a0c7545d15990b5 and manufactured by NEXOBIO Co., Ltd.. The authorized representative in Taiwan is HSIN HUI MEDICAL CO., LTD..
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