Taiwan FDA registration 0b361bac4dc90fbcb1e3648409ed0f1b

"Translite" Liquid crystal vein locator (Non-Sterile)

TW: "崔萊特" 液晶靜脈定位器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TRANSLITE LLC·Registered May 12, 2016 – May 12, 2026Expired
Registration details
Analysis ID
0b361bac4dc90fbcb1e3648409ed0f1b
License Form
Ministry of Health Medical Device Import No. 016524
Customs Code
DHA09401652404
Company information
Manufacturer
TRANSLITE LLC
Manufacturer Country
United States
Authorized Representative
DENSO SCIENTIFIC CO., LTD.
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
May 12, 2016
Expiry Date
May 12, 2026
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About this record

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 0b361bac4dc90fbcb1e3648409ed0f1b and manufactured by TRANSLITE LLC. The authorized representative in Taiwan is DENSO SCIENTIFIC 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.

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