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Kendall

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kendall FDA UDI
Generic Name
Multi-chamber venous compression system garment, reprocessed FDA UDI
Device Name
KENDALL SCD Express Sleeves. This product is designed for use with KENDALL SCD SMARTFLOW Controller. Knee Length Medium Single Patient Use. Kit Contents: 83022 and/or 83022R. May Contain OEM and/or Reprocessed Devices. Exposed to EO Gas. Reprocessed Device for Single Patient Use Reprocessed by Sustainable Technologies. FDA UDI
Model / Reference
83022B FDA UDI
Description
KENDALL SCD Express Sleeves. This product is designed for use with KENDALL SCD SMARTFLOW Controller. Knee Length Medium Single Patient Use. Kit Contents: 83022 and/or 83022R. May Contain OEM and/or Reprocessed Devices. Exposed to EO Gas. Reprocessed Device for Single Patient Use Reprocessed by Sustainable Technologies. FDA UDI

Identifiers

Catalog Number
83022B FDA UDI
Primary DI / UDI-DI
50885380194595 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Multi-chamber venous compression system garment, reprocessed 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

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: Multi-chamber venous compression system garment, reprocessed

Kendall by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 723946ba-0ec2-4fa9-9853-ca9c7f26ae07 34 fields · synced Jun 8, 2026