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Edwards SAPIEN 3 Ultra Transcatheter Heart Valve

FDA UDI

Class III (US FDA UDI)

by Edwards Lifesciences LLC

Identity

Trade Name
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve FDA UDI
Model / Reference
9750TFX26 FDA UDI
Description
Edwards SAPIEN 3 Ultra Transcatheter Heart Valve FDA UDI

Identifiers

Catalog Number
9750TFX26A FDA UDI
Primary DI / UDI-DI
00690103201338 FDA UDI
PMA Number
P140031 FDA UDI
FDA Product Code
NPU FDA UDI
NPT FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Vascular catheter introduction set, nonimplantableCatheter/overtube balloon inflator, single-useAortic transcatheter heart valve bioprosthesis, stent-like frameworkMitral transcatheter heart valve bioprosthesis

Edwards SAPIEN 3 Ultra Transcatheter Heart Valve by Edwards Lifesciences LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic crimper.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7425b7bd-8e86-4f94-95f6-053ff9c8dd36 38 fields · synced Jun 8, 2026