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Leader

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 110, Inc.

Identity

Trade Name
LEADER FDA UDI
Generic Name
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
LDR Sterile Transparent Waterseal Dressing 4in x 4.75in 4 ea FDA UDI
Model / Reference
5736392 FDA UDI
Description
LDR Sterile Transparent Waterseal Dressing 4in x 4.75in 4 ea FDA UDI

Identifiers

Catalog Number
5736392 FDA UDI
Primary DI / UDI-DI
00096295141177 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive 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

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

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

Dimensions & Sizes

Size
Width — 4 Inch FDA UDI
Length — 4.75 Inch FDA UDI

Category: Antimicrobial synthetic polymer semi-permeable film dressing, adhesive

Leader by Cardinal Health 110, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antimicrobial synthetic polymer semi-permeable film dressing, adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 110, Inc.

Sources (1)

  • FDA UDI decc2ac6-75c3-441a-8970-b26b6688f23c 37 fields · synced Jun 1, 2026