Taiwan FDA registration cd6110ba0175170769300b01c69723a6
"KDLAY" balloon dilation pressure pump
TW: "康德萊" 球囊擴張壓力泵
Registration details
- Analysis ID
- cd6110ba0175170769300b01c69723a6
- Customs Code
- DHA09200163202
Company information
- Manufacturer
- Shanghai Kindly Medical Instruments Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- Dr. Diamond 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.1650 血管攝影注射器和注射筒
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 24, 2024
- Expiry Date
- Nov 24, 2029
About this record
Access comprehensive regulatory information for "KDLAY" balloon dilation pressure pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cd6110ba0175170769300b01c69723a6 and manufactured by Shanghai Kindly Medical Instruments Co., Ltd. The authorized representative in Taiwan is Dr. Diamond 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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