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TIDIShield

FDA UDI

Class I (US FDA UDI)

by Tidi Products, Llc

Identity

Trade Name
TIDIShield FDA UDI
Generic Name
Eye splash shield, single-use FDA UDI
Device Name
Assemble 'n Go Faceshield Replaccement Lenses FDA UDI
Model / Reference
2210-100 FDA UDI
Description
Assemble 'n Go Faceshield Replaccement Lenses FDA UDI

Identifiers

Catalog Number
2210-100 FDA UDI
Primary DI / UDI-DI
00618125128648 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Eye 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Eye splash shield, single-use

TIDIShield by Tidi Products, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye splash shield, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tidi Products, Llc

Sources (1)

  • FDA UDI b65e92f1-bde6-495d-a834-e79ac6b8044b 34 fields · synced Jun 1, 2026