Safety Needle

GUDID 05907527942088

STERIPACK MEDICAL POLAND SP Z O O

Hypodermic needle, single-use
Primary Device ID05907527942088
NIH Device Record Key20848b8a-ea58-425a-823d-c50b841701b2
Commercial Distribution StatusIn Commercial Distribution
Brand NameSafety Needle
Version Model NumberSafety Needle 22Gx1
Company DUNS522155365
Company NameSTERIPACK MEDICAL POLAND SP Z O O
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS105907527942088 [Primary]

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 Number4
Public Version Date2019-11-11
Device Publish Date2018-10-22

On-Brand Devices [Safety Needle]

05907527942194Safety Needle 20Gx1 1/2
05907527942095Safety Needle 22Gx1 1/2
05907527942088Safety Needle 22Gx1
05907527942033Safety Needle 22Gx1 1/2
05907527942026Safety Needle 23Gx1
059075279421877527942187
059075279420717527942071
059075279420647527942064
059075279420197527942019
059075279420027527942002

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