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Etnia Eyewear Culture

FDA UDI

Class I (US FDA UDI)

by Etnia Barcelona, Llc.

Identity

Trade Name
Etnia Eyewear Culture FDA UDI
Generic Name
Spectacle frame FDA UDI
Device Name
Frame Spectacle FDA UDI
Model / Reference
8 DICKE 49O 25 BLH/P FDA UDI
Description
Frame Spectacle FDA UDI

Identifiers

Primary DI / UDI-DI
08435685086483 FDA UDI
FDA Product Code
HQZ FDA UDI
GMDN Term
Spectacle frame FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5842 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Spectacle frame

Etnia Eyewear Culture by Etnia Barcelona, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spectacle frame.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f8b94b74-7461-4fb6-a4ab-c99476fd835c 34 fields · synced May 30, 2026