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Kendall

FDA UDI

Class U (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Wound irrigation sterile saline FDA UDI
Device Name
Sterile Saline Wound Solution FDA UDI
Model / Reference
210SAL FDA UDI
Description
Sterile Saline Wound Solution FDA UDI

Identifiers

Catalog Number
210SAL FDA UDI
Primary DI / UDI-DI
20884521139753 FDA UDI
510(k) Number
K083042 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound irrigation sterile saline FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

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: Wound irrigation sterile saline

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

Similar devices

Also classified as Wound irrigation sterile saline.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 8f3d1e8e-3f5d-42f0-9f99-b6b6f07a8311 38 fields · synced May 30, 2026