← Back to catalogue

McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Urinary catheter holder FDA UDI
Device Name
Catheter Securement Device FDA UDI
Model / Reference
172-5445-9 FDA UDI
Description
Catheter Securement Device FDA UDI

Identifiers

Primary DI / UDI-DI
00612479223639 FDA UDI
FDA Product Code
EYJ FDA UDI
GMDN Term
Urinary catheter holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5130 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urinary catheter holder

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

Similar devices

Also classified as Urinary catheter holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 668752b7-5933-47c2-95a4-19faaee56011 33 fields · synced May 30, 2026