Taiwan FDA registration 387684070b6e3afc3e7a473dfaa9c667
"Caifa" pressure lines and their accessories (unsterilized)
TW: “才發” 壓力管路及其附件 (未滅菌)
Taiwan·Risk Class 1·TSAIR FA INDUSTRIAL DESIGN CO.·Registered Oct 18, 2012 – Oct 18, 2022CancelledRegistration details
- Analysis ID
- 387684070b6e3afc3e7a473dfaa9c667
Company information
- Manufacturer
- TSAIR FA INDUSTRIAL DESIGN CO.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TSAIR FA INDUSTRIAL DESIGN CO.
Product details
- Intended Use
- Limited to the first level identification range of pressure pipelines and their accessories (D.5860) of the management measures for medical equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5860 Pressure lines and accessories thereof
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 18, 2012
- Expiry Date
- Oct 18, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Caifa" pressure lines and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 387684070b6e3afc3e7a473dfaa9c667 and manufactured by TSAIR FA INDUSTRIAL DESIGN CO.. The authorized representative in Taiwan is TSAIR FA INDUSTRIAL DESIGN CO..
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