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Filac

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Filac FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
3000 ADA Electronic Thermometer,Rectal Complete System with 9' (2.7 m) Cord FDA UDI
Model / Reference
505087 FDA UDI
Description
3000 ADA Electronic Thermometer,Rectal Complete System with 9' (2.7 m) Cord FDA UDI

Identifiers

Catalog Number
505087 FDA UDI
Primary DI / UDI-DI
10884521141216 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 9 Feet FDA UDI

Category: Intermittent electronic patient thermometer

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

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI b22c8801-c32f-49db-ac26-16517cae9de1 37 fields · synced May 29, 2026