Taiwan FDA registration ea6f82707e37a895584579d34a5edb43
"TPMT" Defibrillation Electrode (Non-Sterile)
TW: "台醫" 去顫用電擊貼片
Taiwan·Risk Class 2·MD·ADVANCED MEDICAL DESIGN CO., LTD.·Registered Mar 17, 2022 – Mar 17, 2027ActiveRegistration details
- Analysis ID
- ea6f82707e37a895584579d34a5edb43
- License Form
- Ministry of Health Medical Device Manufacturing No. 007427
Company information
- Manufacturer
- ADVANCED MEDICAL DESIGN CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E5300 DC Defibrillator (with shock plate)
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Mar 17, 2022
- Expiry Date
- Mar 17, 2027
About this record
Access comprehensive regulatory information for "TPMT" Defibrillation Electrode (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea6f82707e37a895584579d34a5edb43 and manufactured by ADVANCED MEDICAL DESIGN CO., LTD.. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..
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