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DeRoyal

FDA UDI

Class II (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Liquid-crystal patient thermometer, single-use FDA UDI
Device Name
SensoStrip Temperature Indicator FDA UDI
Model / Reference
81-010001 FDA UDI
Description
SensoStrip Temperature Indicator FDA UDI

Identifiers

Primary DI / UDI-DI
00749756049856 FDA UDI
FDA Product Code
KPD FDA UDI
GMDN Term
Liquid-crystal patient thermometer, single-use 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Liquid-crystal patient thermometer, single-use

DeRoyal by Deroyal Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liquid-crystal patient thermometer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Deroyal Industries, Inc.

Sources (1)

  • FDA UDI 9c0f3411-0d54-4154-a60c-cf69c5db5b1b 34 fields · synced Jun 8, 2026