Taiwan FDA registration 464e0f6322972cd09e482fde2aa035df
"Pumei" hemostats
TW: "普美" 止血鉗
Registration details
- Analysis ID
- 464e0f6322972cd09e482fde2aa035df
- Customs Code
- DHA04400213105
Company information
- Manufacturer
- PRO-MED INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, LTD.
Product details
- Intended Use
- It is a manual instrument for general surgery, and a kind of non-powered, hand-held or hand-operated surgical hemostat.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- 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" hemostats in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 464e0f6322972cd09e482fde2aa035df 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