← Back to catalogue

Face Shield

FDA UDI

Class I (US FDA UDI)

by Aakron Rule Corp.

Identity

Trade Name
Face Shield FDA UDI
Generic Name
Face splash shield, reusable FDA UDI
Model / Reference
43251 FDA UDI

Identifiers

Primary DI / UDI-DI
00850021384005 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Face splash shield, reusable 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Face splash shield, reusable

Face Shield by Aakron Rule Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Face splash shield, 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
Aakron Rule Corp.

Sources (1)

  • FDA UDI c7ad4c02-2052-4617-9f85-9848529f04b2 32 fields · synced May 30, 2026