Taiwan FDA registration 87ae6bdca0b27dce12e1bc23944fd042
"Edfens" osmotic pressure analyzer
TW: “愛德芬斯”滲透壓分析儀
Taiwan·Risk Class 1·ADVANCED INSTRUMENTS, INC·Registered Oct 03, 2005 – Oct 03, 2010CancelledRegistration details
- Analysis ID
- 87ae6bdca0b27dce12e1bc23944fd042
- Customs Code
- DHA04400071001
Company information
- Manufacturer
- ADVANCED INSTRUMENTS, INC
- Manufacturer Country
- United States
- Authorized Representative
- BIOWAY CORPORATION
Product details
- Intended Use
- The osmometer used in clinical practice is a device that measures the osmotic pressure of bodily fluids, which can be determined by means such as freezing point measurement, and is used to diagnose and treat abnormalities in bodily fluids.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 2010
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Edfens" osmotic pressure analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87ae6bdca0b27dce12e1bc23944fd042 and manufactured by ADVANCED INSTRUMENTS, INC. The authorized representative in Taiwan is BIOWAY CORPORATION.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices