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McKesson

FDA UDI

Class I (US FDA UDI)

by Advanced Medical Solutions Limited

Identity

Trade Name
McKesson FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial FDA UDI
Device Name
41-2AP - High Performance Dressing FDA UDI
Model / Reference
High Performance Dressing FDA UDI
Description
41-2AP - High Performance Dressing FDA UDI

Identifiers

Catalog Number
87200 FDA UDI
Primary DI / UDI-DI
10612479243511 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

McKesson by Advanced Medical Solutions Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9f401c9c-6865-4025-b239-8e44759c4ed6 34 fields · synced Jun 1, 2026