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Kendall

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
Pharmaceutical Waste Container Non-Biohazard,Hinged Lid with Snap Cap FDA UDI
Model / Reference
8820NB FDA UDI
Description
Pharmaceutical Waste Container Non-Biohazard,Hinged Lid with Snap Cap FDA UDI

Identifiers

Catalog Number
8820NB FDA UDI
Primary DI / UDI-DI
20884521141596 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Sharps container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 2 Gallon FDA UDI

Category: Sharps container

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

Similar devices

Also classified as Sharps container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI b577cef1-9a47-4dbf-9feb-05c54abeb00b 36 fields · synced May 31, 2026