← Back to catalogue

Good Sense

FDA UDI

Class II (US FDA UDI)

by Geiss, Destin & Dunn, Inc

Identity

Trade Name
Good Sense FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Good SenseTemple Touch Mini Thermometer FDA UDI
Model / Reference
69-330 FDA UDI
Description
Good SenseTemple Touch Mini Thermometer FDA UDI

Identifiers

Catalog Number
69-330 FDA UDI
Primary DI / UDI-DI
00846036007343 FDA UDI
510(k) Number
K032362 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, skin 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

No

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: Infrared patient thermometer, skin

Good Sense by Geiss, Destin & Dunn, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 228e428a-8290-4a26-8de0-3ceb538e3a7c 36 fields · synced May 30, 2026