Taiwan FDA registration f4c7932364bda5fda286243363f4248f
"Zhongpeng" follicular egg retrieval needle/needle set
TW: "中朋" 濾泡取卵針/針組
Taiwan·Risk Class 2·LABOTECT LABOR-TECHNIK-GÖTTINGEN GMBH·Registered Nov 16, 2005 – Nov 16, 2015CancelledRegistration details
- Analysis ID
- f4c7932364bda5fda286243363f4248f
- Customs Code
- DHA00601297708
Company information
- Manufacturer
- LABOTECT LABOR-TECHNIK-GÖTTINGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Zhongpeng Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Import Information
- import
Dates and status
- Registration Date
- Nov 16, 2005
- Expiry Date
- Nov 16, 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 "Zhongpeng" follicular egg retrieval needle/needle set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4c7932364bda5fda286243363f4248f and manufactured by LABOTECT LABOR-TECHNIK-GÖTTINGEN GMBH. 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