AMMEX Professional

GUDID 00697383110817

Case

AMMEX CORPORATION

Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Primary Device ID00697383110817
NIH Device Record Key8981d63f-0cb3-4e81-8459-cdbbd58d70fe
Commercial Distribution StatusIn Commercial Distribution
Brand NameAMMEX Professional
Version Model NumberAPFN42100
Company DUNS187070768
Company NameAMMEX CORPORATION
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100697383110817 [Primary]

FDA Product Code

LZAPolymer Patient Examination Glove

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-27
Device Publish Date2022-07-19

On-Brand Devices [AMMEX Professional]

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00697383959447Case
00697383959119Box
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00697383500427Box
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00697383410429Case
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00697383410405Case
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00697383400413Box
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00697383110848Case
00697383110831Case
00697383110824Case
00697383110817Case
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00697383411044Case
00697383411037Case
00697383411020Case
00697383411013Case
00697383401045Box
00697383401021Box

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