Taiwan FDA registration fb14c8220f8d0d3348e0c72f281aa674

"Otto" myocardial lead

TW: "奧圖" 心肌導線
Taiwan flagTaiwan·Risk Class 2·ALTO DEVELOPMENT CORPORATION·Registered Feb 19, 2002 – Feb 19, 2027Active
Registration details
Analysis ID
fb14c8220f8d0d3348e0c72f281aa674
Customs Code
DHA00600982705
Company information
Manufacturer Country
United States
Authorized Representative
ZIMMER BIOMET TAIWAN CO., LTD.
Product details
Intended Use
Vacuum.
Product Type (Level 1)
E Cardiovascular Medicine Science
Dates and status
Registration Date
Feb 19, 2002
Expiry Date
Feb 19, 2027
About this record

Access comprehensive regulatory information for "Otto" myocardial lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb14c8220f8d0d3348e0c72f281aa674 and manufactured by ALTO DEVELOPMENT CORPORATION. The authorized representative in Taiwan is ZIMMER BIOMET 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