Taiwan FDA registration 89f9a2bdfa50fbd2000fb8bc51ce2648
"Sendega Technology" Insay peristaltic pressure test device
TW: "森德賀科技" 茵賽蠕動壓測試裝置
Registration details
- Analysis ID
- 89f9a2bdfa50fbd2000fb8bc51ce2648
- Customs Code
- DHA00601026502
Company information
- Manufacturer
- SANDHILL SCIENTIFIC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Kaiju Limited
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2003
- Expiry Date
- Apr 03, 2018
- Cancellation Date
- Dec 09, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sendega Technology" Insay peristaltic pressure test device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 89f9a2bdfa50fbd2000fb8bc51ce2648 and manufactured by SANDHILL SCIENTIFIC, INC.. The authorized representative in Taiwan is Kaiju Limited.
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.
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