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Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Suction system bottle FDA UDI
Device Name
Cardinal Health Lukens Tube 20CC, 6 1/4" FDA UDI
Model / Reference
19510-065 FDA UDI
Description
Cardinal Health Lukens Tube 20CC, 6 1/4" FDA UDI

Identifiers

Catalog Number
19510-065 FDA UDI
Primary DI / UDI-DI
10885380138232 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
Suction system bottle 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 6.25 Inch FDA UDI
Total Volume — 20 Milliliter FDA UDI

Category: Suction system bottle

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

Similar devices

Also classified as Suction system bottle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 57e38ea7-0ee7-490d-a454-96d8538cbd75 35 fields · synced Jun 8, 2026