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Foster & Thrive

FDA UDI

Class II (US FDA UDI)

by Mckesson Corp.

Identity

Trade Name
Foster & Thrive FDA UDI
Generic Name
Electronic thermometer probe cover FDA UDI
Device Name
50 pack of probe covers. A device intended to be used as a physical barrier between the patient and the probe of a thermometer to prevent cross-contamination between patients. This is a single-use device. FDA UDI
Model / Reference
K-955.F&T FDA UDI
Description
50 pack of probe covers. A device intended to be used as a physical barrier between the patient and the probe of a thermometer to prevent cross-contamination between patients. This is a single-use device. FDA UDI

Identifiers

Primary DI / UDI-DI
00010939960207 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Electronic thermometer probe cover 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electronic thermometer probe cover

Foster & Thrive by Mckesson Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic thermometer probe cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Corp.

Sources (1)

  • FDA UDI 505fd3e3-7f27-4a3f-bcc2-b8d6710167e0 34 fields · synced May 30, 2026