"TRANSLITE" Liquid crystal vein locator (Non-Sterile)
- Analysis ID
- a4fec8aae6f64a4cb5a96e451b8d15e8
- License Form
- Ministry of Health Medical Device Import No. 017807
- Customs Code
- DHA09401780708
- Manufacturer
- TRANSLITE LLC
- Manufacturer Country
- United States
- Authorized Representative
- SMART LIFE INTERNATIONAL 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 10, 2017
- Expiry Date
- May 10, 2027
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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 a4fec8aae6f64a4cb5a96e451b8d15e8 and manufactured by TRANSLITE LLC. The authorized representative in Taiwan is SMART LIFE INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including TRANSLITE LLC, TRANSLITE, 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.