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Medi-First Plastic Strip 20 count

FDA UDI

Class I (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Plastic Strip 20 count FDA UDI
Generic Name
Skin-cover adhesive strip, non-antimicrobial FDA UDI
Device Name
A sterile piece of beige plastic material,with an absorbent pad, intended to be applied to a part of a patient's body and held in place by its pressure-sensitive adhesive to cover and protect wounds FDA UDI
Model / Reference
66171 FDA UDI
Description
A sterile piece of beige plastic material,with an absorbent pad, intended to be applied to a part of a patient's body and held in place by its pressure-sensitive adhesive to cover and protect wounds FDA UDI

Identifiers

Catalog Number
66171 FDA UDI
Primary DI / UDI-DI
00347682661717 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-cover adhesive strip, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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: Skin-cover adhesive strip, non-antimicrobial

Medi-First Plastic Strip 20 count by Medique Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-cover adhesive strip, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI 81fe0f56-b04e-48e5-aee1-d5e987c1cb5c 35 fields · synced May 30, 2026