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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
General-purpose surgical suction system, vacuum FDA UDI
Device Name
Mucus Trap with Vacuum Breaker and Filter,6.5 Fr/Ch (2.2 mm), Catheter FDA UDI
Model / Reference
8888257485 FDA UDI
Description
Mucus Trap with Vacuum Breaker and Filter,6.5 Fr/Ch (2.2 mm), Catheter FDA UDI

Identifiers

Catalog Number
8888257485 FDA UDI
Primary DI / UDI-DI
20884527000163 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
General-purpose surgical suction system, vacuum FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 20 Milliliter FDA UDI
Catheter Gauge — 6.5 French FDA UDI

Category: General-purpose surgical suction system, vacuum

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

Similar devices

Also classified as General-purpose surgical suction system, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI dfa0a5d9-d84b-42b2-b4e6-9072bfe893f8 36 fields · synced May 30, 2026