Taiwan FDA registration 0a19e64024cdce2e581b7ac9e73061db
"Apt" Zurich guide line
TW: “埃普特”蘇黎世導引線
Taiwan·Risk Class 2·APT Medical Inc.·Registered Apr 23, 2022 – Apr 23, 2027ActiveRegistration details
- Analysis ID
- 0a19e64024cdce2e581b7ac9e73061db
- Customs Code
- DHA09200133302
Company information
- Manufacturer
- APT Medical Inc.
- Manufacturer Country
- China
- Authorized Representative
- NO.1 BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1330 Catheter Guide Wires
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 23, 2022
- Expiry Date
- Apr 23, 2027
About this record
Access comprehensive regulatory information for "Apt" Zurich guide line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a19e64024cdce2e581b7ac9e73061db and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY 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.
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