← Back to catalogue

Dagamma

FDA UDI

Class II (US FDA UDI)

by Dagamma Inc.

Identity

Trade Name
Dagamma FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
DT1000 Digital Infrared Forehead and Ear Thermometer by Dagamma FDA UDI
Model / Reference
DT1000 FDA UDI
Description
DT1000 Digital Infrared Forehead and Ear Thermometer by Dagamma FDA UDI

Identifiers

Primary DI / UDI-DI
00628055787259 FDA UDI
510(k) Number
K131243 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infrared patient thermometer, skinInfrared patient thermometer, ear

Dagamma by Dagamma Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, ear.

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

Manufacturer
Dagamma Inc.

Sources (1)

  • FDA UDI 6a1eff42-bc96-4c57-a717-a888e1d09f59 35 fields · synced May 30, 2026