Taiwan FDA registration e99e3812cf8a31aab515d047a6d267ab
"Epter" Detrik double-cavity microtubules
TW: “埃普特” 德萃克雙腔微導管
Taiwan·Risk Class 2·APT Medical Inc.·Registered Jul 11, 2024 – Jul 11, 2029ActiveRegistration details
- Analysis ID
- e99e3812cf8a31aab515d047a6d267ab
- Customs Code
- DHA09200158302
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.1250 Percutaneous catheters
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 11, 2024
- Expiry Date
- Jul 11, 2029
About this record
Access comprehensive regulatory information for "Epter" Detrik double-cavity microtubules in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e99e3812cf8a31aab515d047a6d267ab and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..
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