AMPMED

GUDID 00810477022821

AMPLIM, LLC

Infrared patient thermometer, skin
Primary Device ID00810477022821
NIH Device Record Key6038e37e-5edd-4471-a9f6-b338bcc97cec
Commercial Distribution StatusIn Commercial Distribution
Brand NameAMPMED
Version Model NumberAMP1701
Company DUNS080521945
Company NameAMPLIM, LLC
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100810477022821 [Primary]

FDA Product Code

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 Date2020-03-25
Device Publish Date2020-03-17

On-Brand Devices [AMPMED]

00810477022197AMP1701
00810477022180AMP1701
00810477022319AMP1910
08104770219098AMP1812
00810477021909AMP1812
00810477021749AMP1701
00810477021558AMP1701
00810477022791AMP1910
00810477022302AMP1907
00810477022296AMP1907
00810477022852AMP701
00810477022845AMP1701
00810477022838AMP1701
00810477022821AMP1701
00810477022807AMP1701

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