Taiwan FDA registration 121680979dd46a3fc3a7aa623930d48d
"Biogulu" surgical gel
TW: “拜歐古陸”手術凝膠
Taiwan·Risk Class 3·CRYOLIFE INC·Registered May 25, 2009 – May 25, 2024CancelledRegistration details
- Analysis ID
- 121680979dd46a3fc3a7aa623930d48d
- Customs Code
- DHA00602001906
Company information
- Manufacturer
- CRYOLIFE INC
- Manufacturer Country
- United States
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- BioGlue Surgical Gel is used in adult patients to assist standard hemostasis methods (e.g. sutures, surgical staples) when surgically repairing large blood vessels (e.g., aorta, femoral artery and carotid artery).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- May 25, 2009
- Expiry Date
- May 25, 2024
- Cancellation Date
- Nov 06, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Biogulu" surgical gel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 121680979dd46a3fc3a7aa623930d48d and manufactured by CRYOLIFE INC. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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