← Back to catalogue

Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Secretion suction kit FDA UDI
Device Name
Tracheostomy Care Tray FDA UDI
Model / Reference
47885 FDA UDI
Description
Tracheostomy Care Tray FDA UDI

Identifiers

Catalog Number
47885 FDA UDI
Primary DI / UDI-DI
10884527000272 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Secretion suction kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Secretion suction kit

Argyle by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secretion suction kit.

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

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 7bcda888-fef8-4c0e-8889-344a2f04c0f2 36 fields · synced Jun 8, 2026