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ThruPort Systems QuickDraw Venous Cannula with Insertion Kit

FDA UDI

Class II (US FDA UDI)

by Edwards Lifesciences LLC

Identity

Trade Name
ThruPort Systems QuickDraw Venous Cannula with Insertion Kit FDA UDI
Generic Name
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI
Device Name
ThruPort Systems QuickDraw Venous Cannula FDA UDI
Model / Reference
QD25 FDA UDI
Description
ThruPort Systems QuickDraw Venous Cannula FDA UDI

Identifiers

Catalog Number
QD25 FDA UDI
Primary DI / UDI-DI
00690103182705 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 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

Yes

FDA UDI

Combination Product

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: Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage

ThruPort Systems QuickDraw Venous Cannula with Insertion Kit by Edwards Lifesciences LLC — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Edwards Lifesciences LLC

Sources (1)

  • FDA UDI f7260eb5-8a7e-475c-8b13-8b61a6070827 37 fields · synced Jun 8, 2026