Ease®

FDA UDI

Class II (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: EASE MICROFIBER KNEE HIGH - DOT 20-30 mmHg BLACK W/RED DOT LARGE LONG FDA UDI
Model / Reference: 62030 FDA UDI
Description: EASE MICROFIBER KNEE HIGH - DOT 20-30 mmHg BLACK W/RED DOT LARGE LONG FDA UDI

Identifiers

Primary DI / UDI-DI: 00721734620301 FDA UDI
FDA Product Code: DWL FDA UDI
FQL FDA UDI
GMDN Term: Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class: Class II 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 II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Knit-Rite, Inc

Sources (1)

FDA UDI 95e87ce8-38cb-49b3-b5f6-927d21b7d26e 33 fields · synced May 31, 2026