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Argyle

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Argyle FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Device Name
Poole Suction Instrument,Rigid FDA UDI
Model / Reference
8888509703 FDA UDI
Description
Poole Suction Instrument,Rigid FDA UDI

Identifiers

Catalog Number
8888509703 FDA UDI
Primary DI / UDI-DI
10884527019731 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use 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

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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
Length — 25 Centimeter FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, single-use

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

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI a2ade6d6-4de6-4c0b-8ede-2e6d87972ed1 36 fields · synced May 31, 2026