"BOTISS" Endosseous dental implant accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·BOTISS BIOMATERIALS GMBH·Registered Jun 14, 2016 – Jun 14, 2021Cancelled- Analysis ID
- ffa87cc50b777e887e346942eb766ce1
- License Form
- Ministry of Health Medical Device Import No. 016647
- Customs Code
- DHA09401664707
- Manufacturer
- BOTISS BIOMATERIALS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Hongzhan Limited
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
- Registration Date
- Jun 14, 2016
- Expiry Date
- Jun 14, 2021
- Cancellation Date
- Mar 04, 2020
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for "BOTISS" Endosseous dental implant accessories (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 ffa87cc50b777e887e346942eb766ce1 and manufactured by BOTISS BIOMATERIALS GMBH. The authorized representative in Taiwan is Hongzhan Limited.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BOTISS BIOMATERIALS GMBH, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.