← Back to catalogue

AngioVac

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
AngioVac FDA UDI
Generic Name
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI
Device Name
AngioVac C20 with Obturator FDA UDI
Model / Reference
H965251930 FDA UDI
Description
AngioVac C20 with Obturator FDA UDI

Identifiers

Catalog Number
25193 FDA UDI
Primary DI / UDI-DI
15051684016490 FDA UDI
510(k) Number
K190594 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

No

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

AngioVac by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K190594 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Angiodynamics, Inc

Sources (1)

  • FDA UDI 7c0fb2b6-7830-42ce-bfb3-c1bc6c673de7 36 fields · synced Jun 20, 2026