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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Wound dressing kit, medicated FDA UDI
Device Name
TRAY,DRESSING CHANGE FDA UDI
Model / Reference
DYK1101835CV FDA UDI
Description
TRAY,DRESSING CHANGE FDA UDI

Identifiers

Catalog Number
DYK1101835CV FDA UDI
Primary DI / UDI-DI
10080196117505 FDA UDI
FDA Product Code
MCY FDA UDI
GMDN Term
Wound dressing kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound dressing kit, medicated

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound dressing kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e6b86e4-09b3-4485-acca-1a8022f7a6f5 35 fields · synced May 30, 2026