Taiwan FDA registration 1ff7c3bb982ac4fb1dd7515c5ce0badd
"Spiride" embolized spring coil system
TW: “思脈德”栓塞彈簧圈系統
Taiwan·Risk Class 3·Nanjing Sealmedical Technology CO., LTD.;; Shanghai HeartCare Medical Technology Corporation Limited·Registered Oct 18, 2024 – Oct 18, 2029ActiveRegistration details
- Analysis ID
- 1ff7c3bb982ac4fb1dd7515c5ce0badd
- Customs Code
- DHA09200161601
Company information
- Manufacturer
- Nanjing Sealmedical Technology CO., LTD.;; Shanghai HeartCare Medical Technology Corporation Limited
- Manufacturer Country
- China
- Authorized Representative
- BUDDY MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5950 Artificial embolization device
- Import Information
- Chinese goods;; Input;; Contract manufacturing
Dates and status
- Registration Date
- Oct 18, 2024
- Expiry Date
- Oct 18, 2029
About this record
Access comprehensive regulatory information for "Spiride" embolized spring coil system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1ff7c3bb982ac4fb1dd7515c5ce0badd and manufactured by Nanjing Sealmedical Technology CO., LTD.;; Shanghai HeartCare Medical Technology Corporation Limited. The authorized representative in Taiwan is BUDDY MEDICAL CO., LTD..
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