← Back to catalogue

Argyle

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Argyle FDA UDI
Generic Name
Tracheostomy tube neck holder, reusable FDA UDI
Device Name
Argyle Tracheostomy Tube Holder Feature Benefit FDA UDI
Model / Reference
49000 FDA UDI
Description
Argyle Tracheostomy Tube Holder Feature Benefit FDA UDI

Identifiers

Catalog Number
49000 FDA UDI
Primary DI / UDI-DI
10192253044591 FDA UDI
FDA Product Code
CBH FDA UDI
GMDN Term
Tracheostomy tube neck holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 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

Yes

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

No

FDA UDI

Category: Tracheostomy tube neck holder, reusable

Argyle by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube neck holder, reusable.

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 e7b9cae9-a61b-4f0a-b37c-c08f502d5183 34 fields · synced Jun 8, 2026