AMPMED

GUDID 00810477022180

AMPLIM, LLC

Infrared patient thermometer, skin
Primary Device ID00810477022180
NIH Device Record Key4783c029-b3d5-4657-a7dd-a74becc9f9bb
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
GS100810477022180 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FLLThermometer, Electronic, Clinical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-12-09
Device Publish Date2019-05-16

On-Brand Devices [AMPMED]

00810477022197AMP1701
00810477022180AMP1701
00810477022319AMP1910
08104770219098AMP1812
00810477021909AMP1812
00810477021749AMP1701
00810477021558AMP1701
00810477022791AMP1910
00810477022302AMP1907
00810477022296AMP1907
00810477022852AMP701
00810477022845AMP2001J1
00810477022838AMP1701
00810477022821AMP2001W2
00810477022807AMP1701W1
00810477022784AMP1812A
00810477022876AMP2001F2
00810477022883AMP-CA3
00810477022869AMP-CA2
00810477023637AMPAE3W
00810477023620AMPW1W
00810477023613AMPCA3W
00810477023606AMPCA1W
00810477023118AMPW3B
00810477023101AMPW3A
00810477023668AMPCA2W
00810477023651AMPF2W
00810477023125AMP1706
00810477023170AMP1708
00810477023163AMP1707

Trademark Results [AMPMED]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AMPMED
AMPMED
87812567 5575548 Live/Registered
Amplim LLC
2018-02-27

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