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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
Non-wearable adult urine collection bag, closed-ended FDA UDI
Device Name
BAG, URINARY DRAIN, VINYL LF ANTI-REFLUX CHAMBER/FLUTTER VALVE 2000ML FDA UDI
Model / Reference
37-2802 FDA UDI
Description
BAG, URINARY DRAIN, VINYL LF ANTI-REFLUX CHAMBER/FLUTTER VALVE 2000ML FDA UDI

Identifiers

Primary DI / UDI-DI
20612479180691 FDA UDI
FDA Product Code
FAQ FDA UDI
KNX FDA UDI
GMDN Term
Non-wearable adult urine collection bag, closed-ended FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5250 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: Non-wearable adult urine collection bag, closed-ended

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

Similar devices

Also classified as Non-wearable adult urine collection bag, closed-ended.

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 1d4c5f3b-587e-4684-a138-a584f50981b0 33 fields · synced May 30, 2026