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Juzo Custom Compression Garments

FDA UDI

Class I (US FDA UDI)

by Julius Zorn, Inc.

Identity

Trade Name
Juzo Custom Compression Garments FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
18-21 mmHg, Expert, Cotton, Toe Sleeve,Custom FDA UDI
Model / Reference
3021COT.MTM FDA UDI
Description
18-21 mmHg, Expert, Cotton, Toe Sleeve,Custom FDA UDI

Identifiers

Catalog Number
17351 FDA UDI
Primary DI / UDI-DI
00640095173519 FDA UDI
FDA Product Code
FQL 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Juzo Custom Compression Garments by Julius Zorn, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Julius Zorn, Inc.

Sources (1)

  • FDA UDI e4593415-19f6-42c3-9cc6-fbc95007ea7f 35 fields · synced May 31, 2026