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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Hygiene apron, single-use FDA UDI
Device Name
Cystoscopy Apron BLUE PE FILM HEAVY-DUTY Universal FDA UDI
Model / Reference
183-33-8000 FDA UDI
Description
Cystoscopy Apron BLUE PE FILM HEAVY-DUTY Universal FDA UDI

Identifiers

Primary DI / UDI-DI
20612479231997 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Hygiene apron, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

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: Hygiene apron, single-use

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hygiene apron, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI b8241063-dfec-4139-9807-d07ff9c4653a 33 fields · synced Jun 6, 2026