Taiwan FDA registration 2526b734bdc977bd0b7b9f7e074adb53
"Hurricane" Medical absorbent fiber(Non-Sterile)
TW: "賀醫肯" 醫療用吸收纖維(未滅菌)
Taiwan·Risk Class 1·MD·HURRICANE MEDICAL·Registered Feb 08, 2018 – Feb 08, 2028ActiveRegistration details
- Analysis ID
- 2526b734bdc977bd0b7b9f7e074adb53
- License Form
- Ministry of Health Medical Device Import No. 018801
- Customs Code
- DHA09401880101
Company information
- Manufacturer
- HURRICANE MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- EVERLIGHT INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5300 Medical Absorbent Fiber
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 08, 2018
- Expiry Date
- Feb 08, 2028
About this record
Access comprehensive regulatory information for "Hurricane" Medical absorbent fiber(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2526b734bdc977bd0b7b9f7e074adb53 and manufactured by HURRICANE MEDICAL. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT 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 DatabasePowered by Pure Global AI89,000+ Devices