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Juzo Ortho Supports

FDA UDI

Class I (US FDA UDI)

by Julius Zorn, Inc.

Identity

Trade Name
Juzo Ortho Supports FDA UDI
Generic Name
Tubular support bandage, non-latex, reusable FDA UDI
Device Name
Knee Support, Two Lateral Spirals, 2 FDA UDI
Model / Reference
3222DF 2 FDA UDI
Description
Knee Support, Two Lateral Spirals, 2 FDA UDI

Identifiers

Catalog Number
02491 FDA UDI
Primary DI / UDI-DI
00640095024910 FDA UDI
FDA Product Code
IOY FDA UDI
GMDN Term
Tubular support bandage, non-latex, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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: Tubular support bandage, non-latex, reusable

Juzo Ortho Supports by Julius Zorn, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

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 b44eab9d-cfca-4466-885c-b0941f9548cb 35 fields · synced Jun 8, 2026