← Back to catalogue

Juzo SoftCompress

FDA UDI

Class I (US FDA UDI)

by Julius Zorn, Inc.

Identity

Trade Name
Juzo SoftCompress FDA UDI
Generic Name
General-purpose medical foam padding, reusable FDA UDI
Device Name
SoftCompress Liner, Arm , UNI FDA UDI
Model / Reference
6823ACG UNI FDA UDI
Description
SoftCompress Liner, Arm , UNI FDA UDI

Identifiers

Catalog Number
28807 FDA UDI
Primary DI / UDI-DI
00640095288077 FDA UDI
FDA Product Code
MDR FDA UDI
GMDN Term
General-purpose medical foam padding, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5160 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: General-purpose medical foam padding, reusable

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

Similar devices

Also classified as General-purpose medical foam padding, 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
Julius Zorn, Inc.

Sources (1)

  • FDA UDI b5a2fd8f-14ce-4e99-8d6e-4d785a7574be 35 fields · synced Jun 8, 2026