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A&D Medical

FDA UDI

Class II (US FDA UDI)

by A & D Medical

Identity

Trade Name
A&D Medical FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
Digital Thermometer FDA UDI
Model / Reference
DT-105 FDA UDI
Description
Digital Thermometer FDA UDI

Identifiers

Catalog Number
DT-105 FDA UDI
Primary DI / UDI-DI
00093764603129 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Intermittent electronic patient thermometer

A&D Medical by A & D Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A & D Medical

Sources (1)

  • FDA UDI 648b9e11-a4e7-490f-aac8-61571c003eca 35 fields · synced Jun 1, 2026