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Totally Rimless

FDA UDI

Class I (US FDA UDI)

by Mcgee Group, Inc., The

Identity

Trade Name
Totally Rimless FDA UDI
Generic Name
Magnifying spectacles FDA UDI
Device Name
Magnifying Spectacle 52-18-140 (1.25) FDA UDI
Model / Reference
TR Wells Crystal FDA UDI
Description
Magnifying Spectacle 52-18-140 (1.25) FDA UDI

Identifiers

Catalog Number
TRWELLS0CRYS0R125 FDA UDI
Primary DI / UDI-DI
00781096318773 FDA UDI
FDA Product Code
HOI FDA UDI
GMDN Term
Magnifying spectacles FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5840 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: Magnifying spectacles

Totally Rimless by Mcgee Group, Inc., The — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnifying spectacles.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e988449e-b956-4b5c-bf2c-c3b8014aa93b 35 fields · synced May 31, 2026