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Latitude™

FDA UDI

Class I (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
Latitude™ FDA UDI
Generic Name
Face splash shield, single-use FDA UDI
Device Name
Latitude Plus Face Shield (anti-fog) FDA UDI
Model / Reference
32031704 FDA UDI
Description
Latitude Plus Face Shield (anti-fog) FDA UDI

Identifiers

Catalog Number
32031704 FDA UDI
Primary DI / UDI-DI
50009336009942 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Face splash shield, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

No

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: Face splash shield, single-use

Latitude™ by Graphic Controls Acquisition Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Face splash shield, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 025fb379-72f9-479e-84df-ddad13aa6e63 35 fields · synced May 31, 2026