Taiwan FDA registration 29087ccefbeced172a908c8ec6db89f9
"Kostiy" LCD vein locator (unsterilized)
TW: "柯斯堤" 液晶靜脈定位器 (未滅菌)
Registration details
- Analysis ID
- 29087ccefbeced172a908c8ec6db89f9
- Customs Code
- DHA04401169309
Company information
- Manufacturer
- CHRISTIE MEDICAL HOLDINGS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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)
- J.6970 液晶靜脈定位器
- Import Information
- import
Dates and status
- Registration Date
- May 11, 2012
- Expiry Date
- May 11, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kostiy" LCD vein locator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 29087ccefbeced172a908c8ec6db89f9 and manufactured by CHRISTIE MEDICAL HOLDINGS, INC.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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