Hypodermic Needle

GUDID 00616784696430

DYNAREX CORPORATION

Hypodermic needle, single-use
Primary Device ID00616784696430
NIH Device Record Key5e5158b1-bd86-4962-94d4-c41a032bc101
Commercial Distribution StatusIn Commercial Distribution
Brand NameHypodermic Needle
Version Model Number6964
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
GS100616784696416 [Unit of Use]
GS100616784696423 [Primary]
GS100616784696430 [Package]
Contains: 00616784696423
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMINeedle, Hypodermic, Single Lumen

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 [Hypodermic Needle]

006167846976356976
006167846975366975
006167846974376974
006167846973386973
006167846972396972
006167846971306971
006167846970316970
006167846969356969
006167846968366968
006167846967376967
006167846966386966
006167846965396965
006167846964306964
006167846963316963
006167846962326962
006167846961336961
006167846960346960

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