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Medi-First Eye Pads

FDA UDI

Class I (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Eye Pads FDA UDI
Generic Name
Eye pad FDA UDI
Device Name
A pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. FDA UDI
Model / Reference
64470 FDA UDI
Description
A pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. FDA UDI

Identifiers

Catalog Number
64470 FDA UDI
Primary DI / UDI-DI
00347682644703 FDA UDI
FDA Product Code
HMP FDA UDI
GMDN Term
Eye pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4440 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Eye pad

Medi-First Eye Pads by Medique Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI e2bee922-95e5-403a-938c-816ef3d4e689 35 fields · synced May 31, 2026