Taiwan FDA registration 32c5a6ec7219b754ac64c36d03f68519
"Bausch" Occlusal analysis device & accessories (Non-sterile)
TW: "柏斯" 牙科咬合分析裝置及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·DR. JEAN BAUSCH GMBH & CO.KG·Registered Nov 26, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 32c5a6ec7219b754ac64c36d03f68519
- License Form
- Ministry of Health Medical Device Import Registration No. a00025
- Customs Code
- DHA084a0002500
Company information
- Manufacturer
- DR. JEAN BAUSCH GMBH & CO.KG
- Manufacturer Country
- Germany
- Authorized Representative
- E.S.T. BIOTECH INC.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "occlusal paper (F.6140) first level identification range.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F6140 Occlusal paper
Dates and status
- Registration Date
- Nov 26, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for "Bausch" Occlusal analysis device & 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 32c5a6ec7219b754ac64c36d03f68519 and manufactured by DR. JEAN BAUSCH GMBH & CO.KG. The authorized representative in Taiwan is E.S.T. BIOTECH INC..
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