Taiwan FDA registration 97e389fbbac7637f6deb95c25114f6c4
"AccuVein" Vein Viewing Locator (Non-Sterile)
TW: "愛可芬" 靜脈定位器 (未滅菌)
Registration details
- Analysis ID
- 97e389fbbac7637f6deb95c25114f6c4
- License Form
- Ministry of Health Medical Device Import No. 015007
- Customs Code
- DHA09401500705
Company information
- Manufacturer
- ACCUVEIN LLC
- Manufacturer Country
- United States
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- 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
- Mar 17, 2015
- Expiry Date
- Mar 17, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "AccuVein" Vein Viewing 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 97e389fbbac7637f6deb95c25114f6c4 and manufactured by ACCUVEIN LLC. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., 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