Taiwan FDA registration e09ec9ddff7d7b36e1be09eded222874
Joy American Iron Reagent
TW: 喜樂美鐵試劑
Taiwan·Risk Class 1·SYNERMED INTERNATIONAL INC.·Registered Apr 12, 2006 – Apr 12, 2011CancelledRegistration details
- Analysis ID
- e09ec9ddff7d7b36e1be09eded222874
- Customs Code
- DHA04400361302
Company information
- Manufacturer
- SYNERMED INTERNATIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- PUREBLOOD-TECH INTERNATIONAL CORP.
Product details
- Intended Use
- It is used to quantify iron in serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1410 Iron (non-blood matrix) testing system
- Import Information
- import
Dates and status
- Registration Date
- Apr 12, 2006
- Expiry Date
- Apr 12, 2011
- Cancellation Date
- Nov 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Joy American Iron Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e09ec9ddff7d7b36e1be09eded222874 and manufactured by SYNERMED INTERNATIONAL INC.. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..
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