Syringe w/Needle

GUDID 00616784700731

DYNAREX CORPORATION

Hypodermic needle, single-use
Primary Device ID00616784700731
NIH Device Record Key571189fa-5f13-463f-b55a-384b6cca7fe8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSyringe w/Needle
Version Model Number7007
Company DUNS008124539
Company NameDYNAREX CORPORATION
Device Count100
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100616784700717 [Unit of Use]
GS100616784700724 [Primary]
GS100616784700731 [Package]
Contains: 00616784700724
Package: [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMFSyringe, Piston

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-10-23
Device Publish Date2016-09-24

On-Brand Devices [Syringe w/Needle]

006167847016397016
006167847015307015
006167847014317014
006167847013327013
006167847012337012
006167847011347011
006167847010357010
006167847009397009
006167847008307008
006167847007317007
006167847006327006
006167847005337005
006167847004347004
006167847003357003
006167847002367002
006167847001377001
006167847000387000
006167846999366999
006167846998376998
006167846997386997
006167846996396996
006167846995306995
006167846994316994

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