Taiwan FDA registration 1b8ac40d87f290e266a85c6f9dc162b4
"Medizintechnik Gulden" Periotest (Non-Sterile)
TW: "美德固德" 牙科植體穩定度分析儀 (未滅菌)
Taiwan·Risk Class 1·MD·MEDIZINTECHNIK GULDEN E.K.·Registered Jan 17, 2017 – Jan 17, 2022ExpiredRegistration details
- Analysis ID
- 1b8ac40d87f290e266a85c6f9dc162b4
- License Form
- Ministry of Health Medical Device Import No. 017422
- Customs Code
- DHA09401742201
Company information
- Manufacturer
- MEDIZINTECHNIK GULDEN E.K.
- Manufacturer Country
- Germany
- Authorized Representative
- Baobeiya Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures dental handpieces and their accessories (F.4200).
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4200 Dental Handpiece and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 17, 2017
- Expiry Date
- Jan 17, 2022
About this record
Access comprehensive regulatory information for "Medizintechnik Gulden" Periotest (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 1b8ac40d87f290e266a85c6f9dc162b4 and manufactured by MEDIZINTECHNIK GULDEN E.K.. The authorized representative in Taiwan is Baobeiya Technology Co., Ltd.
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