Juzo Night

FDA UDI

Class I (US FDA UDI)

by Julius Zorn, Inc.

Identity

Trade Name: Juzo Night FDA UDI
Generic Name: General-purpose medical foam padding, reusable FDA UDI
Device Name: Juzo Night, Long, Left , 3 FDA UDI
Model / Reference: 6872ACGLLE 3 FDA UDI
Description: Juzo Night, Long, Left , 3 FDA UDI

Identifiers

Catalog Number: 33677 FDA UDI
Primary DI / UDI-DI: 00640095336778 FDA UDI
FDA Product Code: IQO FDA UDI
GMDN Term: General-purpose medical foam padding, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3025 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: General-purpose medical foam padding, reusable

Juzo Night by Julius Zorn, Inc. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Julius Zorn, Inc.

Sources (1)

FDA UDI 6cd06ddc-0468-4ab5-89d2-8eb044a531d8 35 fields · synced Jun 8, 2026