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Martha Stewart

FDA UDI

Class I (US FDA UDI)

by Colors In Optics Ltd.

Identity

Trade Name
Martha Stewart FDA UDI
Generic Name
Tinted non-prescription spectacles FDA UDI
Device Name
Sunglasses FDA UDI
Model / Reference
M STEWART MS214 - BLACK/OATMEAL FDA UDI
Description
Sunglasses FDA UDI

Identifiers

Catalog Number
MS214 OXOAT FDA UDI
Primary DI / UDI-DI
00781268843256 FDA UDI
FDA Product Code
HQY FDA UDI
GMDN Term
Tinted non-prescription spectacles 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

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: Tinted non-prescription spectacles

Martha Stewart by Colors In Optics Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tinted non-prescription spectacles.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da1fb265-e431-488f-b2cf-d0943ee27ec7 35 fields · synced May 31, 2026