DEVICE: SAPIEN 3 Ultra RESILIA (00690103215816)

Device Identifier (DI) Information

SAPIEN 3 Ultra RESILIA
9755RSL26
In Commercial Distribution
9755RSL26A
Edwards Lifesciences LLC
00690103215816
GS1

1
134139174 *Terms of Use
SAPIEN 3 Ultra RESILIA Transcatheter Heart Valve, 26mm
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Device Characteristics

MR Conditional
No
No
Yes
Yes
No
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
60246 Mitral transcatheter heart valve bioprosthesis
An implantable xenograft (e.g., bovine) intended to be used to repair/replace a stenosed or regurgitant mitral heart valve, or previously-implanted mitral heart valve prosthesis, and which is implanted with a catheter via percutaneous access (e.g., transfemoral, transapical) while the heart is beating. It is comprised of the xenograft, processed to render the tissue non-viable, attached to a metal framework (which may be covered with a synthetic polymer material) that is expandable in situ; it may also include a synthetic polymer subannular valve anchoring component. Devices to assist implantation (e.g., catheter, introducer) are typically included.
Active true
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FDA Product Code

[?]
Product Code Product Code Name
NPU Prosthesis, Mitral Valve, Percutaneously Delivered
NPT Aortic Valve, Prosthesis, Percutaneously Delivered
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
P140031 141
P140031 182
No CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
Special Storage Condition, Specify: Do Not Freeze. Store between 10 and 25 Celsius Degrees (50 to 77 Fahrenheit degrees)
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Clinically Relevant Size

[?]
Size Type Text
Device Size Text, specify: Outer Diameter, 26 MM
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Device Record Status

f81c6229-d56e-49cf-a2f6-4f4f7b38196e
May 02, 2025
2
August 25, 2022
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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
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
No
Yes
Yes
Yes
No CLOSE

Customer Contact

[?]
+1(800)822-9637
tech_support@edwards.com
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