← Back to catalogue

Medi-First 4" Compress Bandage

FDA UDI

Class I (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First 4" Compress Bandage FDA UDI
Generic Name
First aid absorbent pad/bandage FDA UDI
Device Name
A non-medicated sterile device in the form of a patch with gauze roll, to include clips, made from non-woven material (e.g., rayon/polyester) and primarily designed to absorb fluids for medical purposes. FDA UDI
Model / Reference
6771B FDA UDI
Description
A non-medicated sterile device in the form of a patch with gauze roll, to include clips, made from non-woven material (e.g., rayon/polyester) and primarily designed to absorb fluids for medical purposes. FDA UDI

Identifiers

Catalog Number
6771B FDA UDI
Primary DI / UDI-DI
00347682677107 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
First aid absorbent pad/bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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: First aid absorbent pad/bandage

Medi-First 4" Compress Bandage by Medique Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid absorbent pad/bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI 5573f472-d13d-46c2-8f90-6f9408bb1bd7 35 fields · synced May 30, 2026