Ease®

FDA UDI

Class I (US FDA UDI)

by Knit-Rite, Inc

Identity

Trade Name: EASE® FDA UDI
Generic Name: Compression/pressure sock/stocking, single-use FDA UDI
Device Name: 20-30 mmHg SHEER EASE THIGH HIGH MEDIUM SHORT SAND FDA UDI
Model / Reference: 64220 FDA UDI
Description: 20-30 mmHg SHEER EASE THIGH HIGH MEDIUM SHORT SAND FDA UDI

Identifiers

Primary DI / UDI-DI: 00721734642204 FDA UDI
FDA Product Code: FQL FDA UDI
DWL FDA UDI
GMDN Term: Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5780 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Compression/pressure sock/stocking, single-use

Ease® by Knit-Rite, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Compression/pressure sock/stocking, single-use.

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MEDI — MEDI MANUFACTURING, INC. · Class II
JOBST Relief — BSN MEDICAL, INC. · Class II
VenoTrain micro — Bauerfeind GmbH & Co. · Class II
VenoTrain soft, AG, Top band silicone micro dots, Ccl2, open toe, L Plus short, Cream — Bauerfeind AG · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Knit-Rite, Inc

Sources (1)

FDA UDI 2ed67f7c-5e51-4f71-918a-60578c650351 33 fields · synced May 31, 2026