← Back to catalogue

Kendall SCD

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kendall SCD FDA UDI
Generic Name
Multi-chamber venous compression system garment, reusable FDA UDI
Device Name
Kendall SCD Express Tear-Away Sleeves, Thigh Length, Large FDA UDI
Model / Reference
73043 FDA UDI
Description
Kendall SCD Express Tear-Away Sleeves, Thigh Length, Large FDA UDI

Identifiers

Catalog Number
73043 FDA UDI
Primary DI / UDI-DI
10192253016086 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Multi-chamber venous compression system garment, reusable 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-chamber venous compression system garment, reusable

Kendall SCD 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, reusable.

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
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 112d5c5d-1963-47fd-8f13-6c437791bf12 34 fields · synced Jun 8, 2026