"Translite" Liquid Crystal Vein Locator (Non-Sterile)
Taiwan·Risk Class 1·MD·TRANSLITE·Registered May 15, 2015 – May 15, 2025Expired- Analysis ID
- 9ec670ddc03303d51863f97b88926a95
- License Form
- Ministry of Health Medical Device Import No. 015226
- Customs Code
- DHA09401522604
- Manufacturer
- TRANSLITE
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
- 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
- Registration Date
- May 15, 2015
- Expiry Date
- May 15, 2025
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Access comprehensive regulatory information for "Translite" 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 9ec670ddc03303d51863f97b88926a95 and manufactured by TRANSLITE. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRANSLITE LLC, and 2 recent registrations in the same category. 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.