Taiwan FDA registration 9cf2d0a1db8738d1435c1b384c23a0cf
"Moritoka" acid-base tube (unsterilized)
TW: "森德賀" 酸鹼測管 (未滅菌)
Taiwan·Risk Class 1·SANDHILL SCIENTIFIC, INC.·Registered Dec 25, 2015 – Dec 25, 2020CancelledRegistration details
- Analysis ID
- 9cf2d0a1db8738d1435c1b384c23a0cf
- Customs Code
- DHA09401601700
Company information
- Manufacturer
- SANDHILL SCIENTIFIC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Kaiju Limited
Product details
- Intended Use
- Limited to the first level identification range of the "pH electrode of the stomach (H.1400)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1400 胃的酸鹼度電極
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 25, 2015
- Expiry Date
- Dec 25, 2020
- Cancellation Date
- Nov 04, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Moritoka" acid-base tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9cf2d0a1db8738d1435c1b384c23a0cf 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.
Free DatabasePowered by Pure Global AI89,000+ Devices