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Full-Length Face Shield

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Full-Length Face Shield FDA UDI
Generic Name
Face splash shield, single-use FDA UDI
Device Name
Full-Length Face Shield FDA UDI
Model / Reference
2209 FDA UDI
Description
Full-Length Face Shield FDA UDI

Identifiers

Primary DI / UDI-DI
00616784220932 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Face splash shield, single-use

Full-Length Face Shield by Dynarex 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

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI a099f24d-0ced-44c0-87c8-833c5c13bcd4 33 fields · synced Jun 1, 2026