Taiwan FDA registration cb43850826446ea2380755ccd207c16e
Medium-assisted reproductive glass microtubules
TW: 中朋輔助生殖玻璃微管
Taiwan·Risk Class 2·Origio Humagen Pipets·Registered Oct 03, 2005 – Oct 03, 2015CancelledRegistration details
- Analysis ID
- cb43850826446ea2380755ccd207c16e
- Customs Code
- DHA00601255001
Company information
- Manufacturer
- Origio Humagen Pipets
- Manufacturer Country
- United States
- Authorized Representative
- Zhongpeng Limited
Product details
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Import Information
- import
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Medium-assisted reproductive glass microtubules in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb43850826446ea2380755ccd207c16e and manufactured by Origio Humagen Pipets. The authorized representative in Taiwan is Zhongpeng 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