Taiwan FDA registration 2fe379303040d950df53d096c6fc221a
"Pumei" ureteral catheter connector (unsterilized)
TW: "普美" 輸尿管導管連接器 (未滅菌)
Taiwan·Risk Class 1·PRO-MED INSTRUMENTE GMBH·Registered Nov 28, 2005 – Nov 28, 2010CancelledRegistration details
- Analysis ID
- 2fe379303040d950df53d096c6fc221a
- Customs Code
- DHA04400213207
Company information
- Manufacturer
- PRO-MED INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, LTD.
Product details
- Intended Use
- A manual urological device used to connect a urethral catheter.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5130 泌尿導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Nov 28, 2005
- Expiry Date
- Nov 28, 2010
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pumei" ureteral catheter connector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2fe379303040d950df53d096c6fc221a and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, 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