DEVICE: EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE (THV) (00690103192070)
Device Identifier (DI) Information
EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE (THV)
9300TFX
In Commercial Distribution
9300TFX23A
Edwards Lifesciences LLC
9300TFX
In Commercial Distribution
9300TFX23A
Edwards Lifesciences LLC
EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE (23MM)
Device Characteristics
MR Conditional | |
No | |
No | |
Yes | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
60245 | Aortic transcatheter heart valve bioprosthesis, stent-like framework |
An implantable xenograft (e.g., bovine, porcine) intended to be used to repair/replace a stenosed and/or regurgitant aortic heart valve, or previously-implanted aortic heart valve prosthesis, and which is designed to be implanted with a catheter via transarterial access (e.g., femoral, subclavian, aortic) or transapical access while the heart is beating. It is comprised of the xenograft, processed to render the tissue non-viable, attached to an expandable metal framework, which is implanted with an included catheter, and when in situ, may be expanded with a balloon or self-expand. Typically devices associated with implantation (e.g., catheter, introducer) are included.
|
Active | true |
60247 | Pulmonary transcatheter heart valve bioprosthesis |
An implantable xenograft (e.g., bovine, porcine) intended to be used to repair/replace a stenosed or regurgitant pulmonary heart valve prosthesis (previously implanted), or native pulmonary valve anatomy that may have been surgically repaired, and which is designed to be implanted with a catheter via vascular access. It may be attached to an expandable metal framework which may be expanded with a balloon or self-expand, and may include other material types (e.g., synthetic polymer). Devices associated with implantation (e.g., catheter, introducer) may be included.
|
Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
NPT | Aortic valve, prosthesis, percutaneously delivered |
NPV | Pulmonary Valve Prosthesis Percutaneously Delivered |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
P130009 | 000 |
P130009 | 034 |
P130009 | 037 |
P130009 | 057 |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Storage Environment Temperature: between 10 and 25 Degrees Celsius |
Clinically Relevant Size
[?]Size Type Text |
---|
Device Size Text, specify: 23 MILIMETER OUTER DIAMETER EXPANDED VALVE |
Device Record Status
a09a4839-161d-4f54-88c5-3035ef855108
July 04, 2022
5
August 30, 2014
July 04, 2022
5
August 30, 2014
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)822-9837
tech_support@edwards.com
tech_support@edwards.com