Taiwan FDA registration 018d4a8acc51e2ae020251e374818378
“AIR TECHNIQUES”Medical Image Storage Device (Non-Sterile)
TW: “亞耳科技”醫學影像儲存裝置 (未滅菌)
Taiwan·Risk Class 1·MD·Air Techniques Inc.·Registered Jun 24, 2020 – Jun 24, 2025ExpiredRegistration details
- Analysis ID
- 018d4a8acc51e2ae020251e374818378
- License Form
- Ministry of Health Medical Device Import No. 021665
- Customs Code
- DHA09402166503
Company information
- Manufacturer
- Air Techniques Inc.
- Manufacturer Country
- United States
- Authorized Representative
- LIANG CHI BIOTECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first-level recognition scope of the Measures for the Administration of Medical Devices "Medical Image Storage Devices (P.2010)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P2010 Medical Image Storage Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 24, 2020
- Expiry Date
- Jun 24, 2025
About this record
Access comprehensive regulatory information for “AIR TECHNIQUES”Medical Image Storage Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 018d4a8acc51e2ae020251e374818378 and manufactured by Air Techniques Inc.. The authorized representative in Taiwan is LIANG CHI BIOTECHNOLOGY 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