Taiwan FDA registration 2966ae721e5b6d139d40e6c9ab1af315
Avery Group Osmotic Analyzers (Unsterilized)
TW: 艾利鐵克集團滲透壓分析儀(未滅菌)
Taiwan·Risk Class 1·ELITechGroup Inc.·Registered Nov 20, 2019 – Nov 20, 2029ActiveRegistration details
- Analysis ID
- 2966ae721e5b6d139d40e6c9ab1af315
- Customs Code
- DHA09402102608
Company information
- Manufacturer
- ELITechGroup Inc.
- Manufacturer Country
- United States
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- It is limited to the first level identification scope of the permeameter (A.2730) for clinical use.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2730 Permeameter for clinical use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Nov 20, 2019
- Expiry Date
- Nov 20, 2029
About this record
Access comprehensive regulatory information for Avery Group Osmotic Analyzers (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2966ae721e5b6d139d40e6c9ab1af315 and manufactured by ELITechGroup Inc.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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