Pure Global

"Spiride" embolized spring coil system - Taiwan Registration 1ff7c3bb982ac4fb1dd7515c5ce0badd

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..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1ff7c3bb982ac4fb1dd7515c5ce0badd
Registration Details
Taiwan FDA Registration: 1ff7c3bb982ac4fb1dd7515c5ce0badd
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Spiride" embolized spring coil system
TW: โ€œๆ€่„ˆๅพทโ€ๆ “ๅกžๅฝˆ็ฐงๅœˆ็ณป็ตฑ
Risk Class 3

Registration Details

1ff7c3bb982ac4fb1dd7515c5ce0badd

DHA09200161601

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience

K.5950 Artificial embolization device

Chinese goods;; Input;; Contract manufacturing

Dates and Status

Oct 18, 2024

Oct 18, 2029