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Devon

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Devon FDA UDI
Generic Name
Medical device adhesive FDA UDI
Device Name
Safety Basin with Metal Feet FDA UDI
Model / Reference
31140372 FDA UDI
Description
Safety Basin with Metal Feet FDA UDI

Identifiers

Catalog Number
31140372 FDA UDI
Primary DI / UDI-DI
20884527018793 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Medical device adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Devon by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI a454c5d8-915d-4db9-8ac9-844d58676180 36 fields · synced Jun 8, 2026