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Vera Bradley

FDA UDI

Class II (US FDA UDI)

by Mcgee Group, Inc., The

Identity

Trade Name
Vera Bradley FDA UDI
Generic Name
Spectacle frame FDA UDI
Device Name
Spectacle Frame, Size 58-16-140 FDA UDI
Model / Reference
VB Sydney Imperial Rose FDA UDI
Description
Spectacle Frame, Size 58-16-140 FDA UDI

Identifiers

Catalog Number
VBSYDN0IMRS58S16 FDA UDI
Primary DI / UDI-DI
00781096536498 FDA UDI
FDA Product Code
HQR FDA UDI
GMDN Term
Spectacle frame FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4100 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: Spectacle frame

Vera Bradley by Mcgee Group, Inc., The — Class II — 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 a4786547-b444-4c5b-8e1d-ab7779194f4d 35 fields · synced May 30, 2026