Taiwan FDA registration 868c735d36262980c87902fe63193021
Vantocel respirator tubing (unsterilized)
TW: “凡妥賽”呼吸器管路 (未滅菌)
Taiwan·Risk Class 1·VITAL SIGNS, INC.·Registered Mar 10, 2010 – Mar 10, 2015CancelledRegistration details
- Analysis ID
- 868c735d36262980c87902fe63193021
- Customs Code
- DHA04400861403
Company information
- Manufacturer
- VITAL SIGNS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing
- Import Information
- import
Dates and status
- Registration Date
- Mar 10, 2010
- Expiry Date
- Mar 10, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Vantocel respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 868c735d36262980c87902fe63193021 and manufactured by VITAL SIGNS, INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, 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