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Kendall

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Irrigation syringe FDA UDI
Device Name
0.9% Sodium Chloride,Flush Syringe, 3 mL Fill, Removable Disinfectant Cap FDA UDI
Model / Reference
CV9923 FDA UDI
Description
0.9% Sodium Chloride,Flush Syringe, 3 mL Fill, Removable Disinfectant Cap FDA UDI

Identifiers

Catalog Number
CV9923 FDA UDI
Primary DI / UDI-DI
30884521183692 FDA UDI
FDA Product Code
NGT FDA UDI
GMDN Term
Irrigation syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Irrigation syringe

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

Similar devices

Also classified as Irrigation syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 5d50d6a3-48e8-4f48-81cc-2b4cb6e72441 37 fields · synced Jun 8, 2026