Taiwan FDA registration 1f4cf538fd379275e7c0d45af2de04cf
"Siemonch" titanium vascular clamp
TW: “希蒙奇”鈦金屬血管夾
Taiwan·Risk Class 2·Symmetry Surgical Vesocclude, LLC;; ROBLING MEDICAL, INC.·Registered Nov 14, 2016 – Nov 14, 2021CancelledRegistration details
- Analysis ID
- 1f4cf538fd379275e7c0d45af2de04cf
- Customs Code
- DHA05602904404
Company information
- Manufacturer Country
- United States
- Authorized Representative
- TBMS INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4300 Implantable Clips
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Nov 14, 2016
- Expiry Date
- Nov 14, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Siemonch" titanium vascular clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1f4cf538fd379275e7c0d45af2de04cf and manufactured by Symmetry Surgical Vesocclude, LLC;; ROBLING MEDICAL, INC.. The authorized representative in Taiwan is TBMS INTERNATIONAL CORPORATION.
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