Beurer 791.48

GUDID 00850018808170

Digital Thermometer

BEURER NORTH AMERICA, L.P.

Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer
Primary Device ID00850018808170
NIH Device Record Key0971a5e5-0080-4032-a57c-f80fba6b581e
Commercial Distribution StatusIn Commercial Distribution
Brand NameBeurer
Version Model NumberFT13
Catalog Number791.48
Company DUNS078497467
Company NameBEURER NORTH AMERICA, L.P.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone1-800-536-0366
Emailinfo@beurer.com
Phone1-800-536-0366
Emailinfo@beurer.com
Phone1-800-536-0366
Emailinfo@beurer.com
Phone1-800-536-0366
Emailinfo@beurer.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850018808170 [Primary]
GS100850018808170 [Primary]
GS100850018808170 [Primary]
GS100850018808170 [Primary]

FDA Product Code

FLLThermometer, Electronic, Clinical
FLLThermometer, Electronic, Clinical
FLLThermometer, Electronic, Clinical
FLLThermometer, Electronic, Clinical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-10
Device Publish Date2020-11-02

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