Taiwan FDA registration 0467d1fea83e5bf850d5a7c3cfafa104
"He Yiken" medical absorbent fiber (unsterilized)
TW: "賀醫肯" 醫療用吸收纖維(未滅菌)
Taiwan·Risk Class 1·HURRICANE MEDICAL INC.·Registered Jul 09, 2008 – Jul 09, 2018CancelledRegistration details
- Analysis ID
- 0467d1fea83e5bf850d5a7c3cfafa104
- Customs Code
- DHA04400689004
Company information
- Manufacturer
- HURRICANE MEDICAL INC.
- 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)
- J.5300 醫療用吸收纖維
- Import Information
- import
Dates and status
- Registration Date
- Jul 09, 2008
- Expiry Date
- Jul 09, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "He Yiken" medical absorbent fiber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0467d1fea83e5bf850d5a7c3cfafa104 and manufactured by HURRICANE MEDICAL INC.. 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