Taiwan FDA registration a3636536fcf06b5a7ad0a662e48b04dd
"Prowei" Microtrauma Mouth Suture (Sterilization)
TW: "普威" 微創傷口縫合器 (滅菌)
Registration details
- Analysis ID
- a3636536fcf06b5a7ad0a662e48b04dd
Company information
- Manufacturer
- Puwei International Co., Ltd. Yilan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Oct 06, 2015
- Expiry Date
- Oct 06, 2025
About this record
Access comprehensive regulatory information for "Prowei" Microtrauma Mouth Suture (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a3636536fcf06b5a7ad0a662e48b04dd and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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