Taiwan FDA registration 0d2432b97b7118c81d6b1b486b908779
GuidOss Collagen membrane matrix
TW: 蓋奧斯 膠原膜
Taiwan·Risk Class 2·MD·NIBEC Co., Ltd·Registered Mar 22, 2016 – Mar 22, 2026ExpiredRegistration details
- Analysis ID
- 0d2432b97b7118c81d6b1b486b908779
- License Form
- Ministry of Health Medical Device Import No. 028339
- Customs Code
- DHA05602833905
Company information
- Manufacturer
- NIBEC Co., Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Straumann Group (Taiwan) Co. 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)
- F3930 Tricalcium phosphate for alveolar bone restoration
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 22, 2016
- Expiry Date
- Mar 22, 2026
About this record
Access comprehensive regulatory information for GuidOss Collagen membrane matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d2432b97b7118c81d6b1b486b908779 and manufactured by NIBEC Co., Ltd. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
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