Taiwan FDA registration 502bda2bc590a8ddc7b061b2bc172e05
"Ept" Konkel anchors balloon dilation catheter
TW: “埃普特”康克爾錨定球囊擴張導管
Taiwan·Risk Class 2·APT Medical Inc.·Registered Oct 23, 2022 – Oct 23, 2027ActiveRegistration details
- Analysis ID
- 502bda2bc590a8ddc7b061b2bc172e05
- Customs Code
- DHA09200139409
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
- Oct 23, 2022
- Expiry Date
- Oct 23, 2027
About this record
Access comprehensive regulatory information for "Ept" Konkel anchors balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 502bda2bc590a8ddc7b061b2bc172e05 and manufactured by APT Medical Inc.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY CO., LTD..
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