Taiwan FDA registration c983787f429879af7bad1227d6ff826e
Edwards osmotic analyzer (unsterilized)
TW: “艾得紛思”滲透壓分析儀(未滅菌)
Taiwan·Risk Class 1·ADVANCED INSTRUMENTS, LLC·Registered Sep 12, 2007 – Sep 12, 2027ActiveRegistration details
- Analysis ID
- c983787f429879af7bad1227d6ff826e
- Customs Code
- DHA04400614905
Company information
- Manufacturer
- ADVANCED INSTRUMENTS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- BIOWAY CORPORATION
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
- import
Dates and status
- Registration Date
- Sep 12, 2007
- Expiry Date
- Sep 12, 2027
About this record
Access comprehensive regulatory information for Edwards osmotic analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c983787f429879af7bad1227d6ff826e and manufactured by ADVANCED INSTRUMENTS, LLC. The authorized representative in Taiwan is BIOWAY CORPORATION.
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