Phoenix Healthcare Solutions LLC PHX-1001

GUDID 00360913010016

Lancets

PHOENIX HEALTHCARE SOLUTIONS, LLC

Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use Blood lancet, single-use
Primary Device ID00360913010016
NIH Device Record Keyf93acf53-d443-4ba6-8c92-5ac2ab057152
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhoenix Healthcare Solutions LLC
Version Model NumberPHX-1001
Catalog NumberPHX-1001
Company DUNS079146847
Company NamePHOENIX HEALTHCARE SOLUTIONS, LLC
Device Count100
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100360913010016 [Primary]
GS110360913010013 [Package]
Package: CASE [100 Units]
In Commercial Distribution
GS180360913010012 [Unit of Use]

FDA Product Code

FMKLancet, Blood

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-09-24
Device Publish Date2021-09-16

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