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A-V Impulse

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
A-V Impulse FDA UDI
Generic Name
Multi-chamber venous compression system garment, single-use FDA UDI
Device Name
True content to be populated as part of rebranding FDA UDI
Model / Reference
5007 FDA UDI
Description
True content to be populated as part of rebranding FDA UDI

Identifiers

Catalog Number
5007- FDA UDI
Primary DI / UDI-DI
20884521101453 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Multi-chamber venous compression system garment, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-chamber venous compression system garment, single-use

A-V Impulse by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-chamber venous compression system garment, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 124bec32-62bb-4774-91a9-5c3303bd5229 34 fields · synced May 30, 2026