Taiwan FDA registration 82dc20519a2445ac27bd3d2d1bac7581
"Neotech" Vein Viewing Locator (Non-Sterile)
TW: "妮爾泰克" 靜脈定位器（未滅菌）
Taiwan·Risk Class 1·MD·NEOTECH PRODUCTS LLC·Registered Nov 15, 2018 – Nov 15, 2028ActiveRegistration details
- Analysis ID
- 82dc20519a2445ac27bd3d2d1bac7581
- License Form
- Ministry of Health Medical Device Import No. 019823
- Customs Code
- DHA09401982303
Company information
- Manufacturer
- NEOTECH PRODUCTS LLC
- Manufacturer Country
- United States
- Authorized Representative
- CHAMP MEDICS 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
- Nov 15, 2018
- Expiry Date
- Nov 15, 2028
About this record
Access comprehensive regulatory information for "Neotech" 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 82dc20519a2445ac27bd3d2d1bac7581 and manufactured by NEOTECH PRODUCTS LLC. The authorized representative in Taiwan is CHAMP MEDICS 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