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Mabis

FDA UDI

Class II (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
MABIS FDA UDI
Generic Name
Continuous electronic patient thermometer, battery-powered FDA UDI
Device Name
60 SECOND DIGITAL THERMOMETER W/BEEPER FAHRENHEIT FDA UDI
Model / Reference
15-691-000 FDA UDI
Description
60 SECOND DIGITAL THERMOMETER W/BEEPER FAHRENHEIT FDA UDI

Identifiers

Catalog Number
15-691-000 FDA UDI
Primary DI / UDI-DI
00767056156913 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Continuous electronic patient thermometer, battery-powered 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: Continuous electronic patient thermometer, battery-powered

Mabis by Dms Holdings, Inc., — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Continuous electronic patient thermometer, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dms Holdings, Inc.,

Sources (1)

  • FDA UDI 6d1ba3e2-1a62-4978-b8ea-b98bde1e199c 34 fields · synced Jun 1, 2026