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FeverScan Ultra

FDA UDI

Class II (US FDA UDI)

by Lcr Hallcrest, Llc.

Identity

Trade Name
FeverScan Ultra FDA UDI
Generic Name
Liquid-crystal patient thermometer, reusable FDA UDI
Device Name
FeverScan Ultra Reusable Forehead Thermometer FDA UDI
Model / Reference
BFT55U FDA UDI
Description
FeverScan Ultra Reusable Forehead Thermometer FDA UDI

Identifiers

Catalog Number
BFT55U FDA UDI
Primary DI / UDI-DI
10815236020398 FDA UDI
FDA Product Code
KPD FDA UDI
GMDN Term
Liquid-crystal patient thermometer, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2200 FDA UDI
Commercial Distribution
Not 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

No

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

FeverScan Ultra by Lcr Hallcrest, Llc. — Class II — 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
Lcr Hallcrest, Llc.

Sources (1)

  • FDA UDI 86acbff4-9b0e-4f6b-b72a-eb907004e49b 37 fields · synced May 30, 2026