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FeverScan Ultra Reusable

FDA UDI

Class II (US FDA UDI)

by Lcr Hallcrest, Llc.

Identity

Trade Name
FeverScan Ultra Reusable FDA UDI
Generic Name
Liquid-crystal patient thermometer, reusable FDA UDI
Device Name
Reusable Forehead Thermometer. FDA UDI
Model / Reference
PFT55U FDA UDI
Description
Reusable Forehead Thermometer. FDA UDI

Identifiers

Catalog Number
PFT55U FDA UDI
Primary DI / UDI-DI
10815236020626 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 Reusable 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 a2d3eb1f-39b0-4a86-9ccf-00354a7303e0 36 fields · synced May 30, 2026