← Back to catalogue

FeverScan

FDA UDI

Class II (US FDA UDI)

by Lcr Hallcrest, Llc.

Identity

Trade Name
FeverScan FDA UDI
Generic Name
Liquid-crystal patient thermometer, reusable FDA UDI
Device Name
Reusable Forehead Thermometers FDA UDI
Model / Reference
BB150 FDA UDI
Description
Reusable Forehead Thermometers FDA UDI

Identifiers

Catalog Number
BB150 FDA UDI
Primary DI / UDI-DI
10815236020671 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
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

Category: Liquid-crystal patient thermometer, reusable

FeverScan by Lcr Hallcrest, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liquid-crystal patient thermometer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Lcr Hallcrest, Llc.

Sources (1)

  • FDA UDI 450bc128-4e48-4012-88e5-d202af69edaa 35 fields · synced Jun 1, 2026