← Back to catalogue

Halyard

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Nasogastric tube holder, noninvasive FDA UDI
Device Name
Nasogastric Tube Fastener Adult Skin-Friendly Adhesive 6x8cm NonWoven Fabric Beige Wrap-around Tube Securement Tab CA/2000 Not made with Natural Rubber Latex Halyard FDA UDI
Model / Reference
55569 FDA UDI
Description
Nasogastric Tube Fastener Adult Skin-Friendly Adhesive 6x8cm NonWoven Fabric Beige Wrap-around Tube Securement Tab CA/2000 Not made with Natural Rubber Latex Halyard FDA UDI

Identifiers

Primary DI / UDI-DI
30885632417119 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Nasogastric tube holder, noninvasive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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: Nasogastric tube holder, noninvasive

Halyard by Owens & Minor Distribution, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric tube holder, noninvasive.

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 e321d064-f524-48c5-8aea-9ab2471e74ab 33 fields · synced May 30, 2026