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Devon

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Devon FDA UDI
Generic Name
Light source adaptor FDA UDI
Device Name
Universal Light Adapter FDA UDI
Model / Reference
31434101 FDA UDI
Description
Universal Light Adapter FDA UDI

Identifiers

Catalog Number
31434101 FDA UDI
Primary DI / UDI-DI
10884521739635 FDA UDI
FDA Product Code
FSY FDA UDI
GMDN Term
Light source adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Light source adaptor

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

Similar devices

Also classified as Light source adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 5305d6ac-5d7d-4b45-8b21-0a5d63acafb9 36 fields · synced May 30, 2026