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Fabco

FDA UDI

Class II (US FDA UDI)

by First Aid Bandage Co Inc

Identity

Trade Name
FABCO FDA UDI
Generic Name
Retina illumination shield FDA UDI
Device Name
Corneal Light Shield FDA UDI
Model / Reference
Q604205 FDA UDI
Description
Corneal Light Shield FDA UDI

Identifiers

Catalog Number
Q604205 FDA UDI
Primary DI / UDI-DI
30634303800275 FDA UDI
FDA Product Code
HOZ FDA UDI
GMDN Term
Retina illumination shield FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4790 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 1 Millimeter FDA UDI
Outer Diameter — 7 Millimeter FDA UDI

Category: Retina illumination shield

Fabco by First Aid Bandage Co Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Retina illumination shield.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
First Aid Bandage Co Inc

Sources (1)

  • FDA UDI 887625d7-3202-44c1-9b60-780d5706a7f5 36 fields · synced Jun 1, 2026