Taiwan FDA registration 3e25a40a44d86171d7150437ebb372ac
"Inspectis" Liquid crystal vein locator (Non-Sterile)
TW: "因斯派迪"液晶靜脈定位器 (未滅菌)
Taiwan·Risk Class 1·MD·INSPECTIS AB·Registered Dec 11, 2018 – Dec 11, 2023ExpiredRegistration details
- Analysis ID
- 3e25a40a44d86171d7150437ebb372ac
- License Form
- Ministry of Health Medical Device Import No. 019905
- Customs Code
- DHA09401990505
Company information
- Manufacturer
- INSPECTIS AB
- Manufacturer Country
- Sweden
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
Product details
- Intended Use
- Limited to the first level identification range of the "liquid crystal vein locator (J.6970)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6970 LCD Vein Locator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 11, 2018
- Expiry Date
- Dec 11, 2023
About this record
Access comprehensive regulatory information for "Inspectis" Liquid crystal vein locator (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 3e25a40a44d86171d7150437ebb372ac and manufactured by INSPECTIS AB. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, 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