Taiwan FDA registration ddd337ce902f7599482a34f066570e2e

"Edward" Carpenter-Edward Peiluwang prosthetic heart valve

TW: “愛德華”卡本特-愛德華沛旅旺人工心瓣膜
Taiwan flagTaiwan·Risk Class 3·Edwards Lifesciences (Singapore) Pte., Ltd.;; EDWARDS LIFESCIENCES LLC·Registered Aug 29, 2017 – Aug 29, 2027Active
Registration details
Analysis ID
ddd337ce902f7599482a34f066570e2e
Customs Code
DHA05603016401
Company information
Manufacturer Country
United States;;Singapore
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.3925 Hypocardial membrane substitutions
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Aug 29, 2017
Expiry Date
Aug 29, 2027
Companies making similar products

Top companies providing products similar to ""Edward" Carpenter-Edward Peiluwang prosthetic heart valve"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Edward" Carpenter-Edward Peiluwang prosthetic heart valve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ddd337ce902f7599482a34f066570e2e and manufactured by Edwards Lifesciences (Singapore) Pte., Ltd.;; EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EDWARDS LIFESCIENCES LLC, and 1 recent registrations in the same category. 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+ Devices1 Competitors1 Recent Registrations