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Eagle Eyes

FDA UDI

Class I (US FDA UDI)

by Eagle Eyes

Identity

Trade Name
Eagle Eyes FDA UDI
Generic Name
Tinted non-prescription spectacle lens FDA UDI
Device Name
LENNOX/S-030-B Sunglass: Clsc Square GNM-GRY - Frame Material: Metal frame w/ CP tips (rubber temples) - Trilenium Polarized Lens- Sunglasses FDA UDI
Model / Reference
81011 FDA UDI
Description
LENNOX/S-030-B Sunglass: Clsc Square GNM-GRY - Frame Material: Metal frame w/ CP tips (rubber temples) - Trilenium Polarized Lens- Sunglasses FDA UDI

Identifiers

Catalog Number
81011 FDA UDI
Primary DI / UDI-DI
00810712014093 FDA UDI
FDA Product Code
HQY FDA UDI
GMDN Term
Tinted non-prescription spectacle lens FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5850 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tinted non-prescription spectacle lens

Eagle Eyes by Eagle Eyes — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tinted non-prescription spectacle lens.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eagle Eyes

Sources (1)

  • FDA UDI 2665bbb8-1221-46d8-aa8b-7baeef94b401 34 fields · synced May 30, 2026