Taiwan FDA registration 516023f2ad889fa389299b89aaa63c68
"Mintec" air leakage tester (unsterilized)
TW: "明泰科"漏氣測試儀(未滅菌)
Taiwan·Risk Class 1·MINNTECH CORPORATION·Registered Mar 28, 2011 – Mar 28, 2016CancelledRegistration details
- Analysis ID
- 516023f2ad889fa389299b89aaa63c68
- Customs Code
- DHA04401009500
Company information
- Manufacturer
- MINNTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Huixing Co., Ltd
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Endoscopes and Their Accessories (H.1500)".
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Mar 28, 2011
- Expiry Date
- Mar 28, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Mintec" air leakage tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 516023f2ad889fa389299b89aaa63c68 and manufactured by MINNTECH CORPORATION. The authorized representative in Taiwan is Huixing Co., Ltd.
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