Taiwan FDA registration 8347b76f973c3f5422aa6092f6f641a1
"Pengwei" disposable vaginal dilator
TW: "鵬維" 拋棄式陰道擴張器
Taiwan·Risk Class 2·PENG WAVES ENTERPRISE CO., LTD.·Registered Oct 27, 2005 – Oct 27, 2015CancelledRegistration details
- Analysis ID
- 8347b76f973c3f5422aa6092f6f641a1
- Customs Code
- DHY00500155404
Company information
- Manufacturer
- PENG WAVES ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PENG WAVES ENTERPRISE CO., LTD.
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
- Domestic
Dates and status
- Registration Date
- Oct 27, 2005
- Expiry Date
- Oct 27, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pengwei" disposable vaginal dilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8347b76f973c3f5422aa6092f6f641a1 and manufactured by PENG WAVES ENTERPRISE CO., LTD.. The authorized representative in Taiwan is PENG WAVES ENTERPRISE 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