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23mm X 29mm X 55cm Ascendra+ Delivery System

FDA UDI

Class III (US FDA UDI)

by Edwards Lifesciences LLC

Identity

Trade Name
23MM X 29MM X 55CM ASCENDRA+ DELIVERY SYSTEM FDA UDI
Generic Name
Cardiac valvuloplasty catheter FDA UDI
Device Name
23MM ASCENDRA+ DELIVERY SYSTEM FDA UDI
Model / Reference
9355AS23 FDA UDI
Description
23MM ASCENDRA+ DELIVERY SYSTEM FDA UDI

Identifiers

Catalog Number
9355AS23A FDA UDI
Primary DI / UDI-DI
00690103193718 FDA UDI
PMA Number
P130009 FDA UDI
FDA Product Code
NPT FDA UDI
GMDN Term
Cardiac valvuloplasty catheter 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiac valvuloplasty catheter

23mm X 29mm X 55cm Ascendra+ Delivery System by Edwards Lifesciences LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac valvuloplasty catheter.

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 5de7e841-2c07-4ead-a4b9-7aee88699fd9 35 fields · synced Jun 8, 2026