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Faced Shield

FDA UDI

Class I (US FDA UDI)

by Guangzhou Hicare Medical Equipment and Materials Co., Ltd

Identity

Trade Name
Faced Shield FDA UDI
Generic Name
Face splash shield, single-use FDA UDI
Model / Reference
Type A FDA UDI

Identifiers

Primary DI / UDI-DI
06971501070509 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Face splash shield, single-use

Faced Shield by Guangzhou Hicare Medical Equipment and Materials Co., Ltd — 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 59544391-f073-4e39-bb3c-51660f905886 32 fields · synced May 30, 2026