Taiwan FDA registration 1ff02fe809ffe3e4575ba55c87ebb01e

"McKovei" Utima 2nd generation main chest expander (unsterilized)

TW: “邁柯唯”烏提碼第二代主胸擴張器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MAQUET CARDIOVASCULAR LLC·Registered Oct 15, 2008 – Oct 15, 2023Expired
Registration details
Analysis ID
1ff02fe809ffe3e4575ba55c87ebb01e
Customs Code
DHA04400712509
Company information
Manufacturer Country
United States
Authorized Representative
GETINGE GROUP TAIWAN CO., LTD.
Product details
Intended Use
Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.4500 心臟血管外科器械
Import Information
import
Dates and status
Registration Date
Oct 15, 2008
Expiry Date
Oct 15, 2023
About this record

Access comprehensive regulatory information for "McKovei" Utima 2nd generation main chest expander (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1ff02fe809ffe3e4575ba55c87ebb01e and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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