CDMA Quality Choice - Mini Pen Needles AN 3590QC

GUDID 00635515959392

For use with injectors for the subcutaneous injection of approved drugs, including insulin

CHAIN DRUG MARKETING ASSOCIATION, INC.

Autoinjector needle
Primary Device ID00635515959392
NIH Device Record Keyc6c9ba1b-fce4-4d6d-b51a-481aac1dc906
Commercial Distribution StatusIn Commercial Distribution
Brand NameCDMA Quality Choice - Mini Pen Needles
Version Model NumberAN 3590QC
Catalog NumberAN 3590QC
Company DUNS011920774
Company NameCHAIN DRUG MARKETING ASSOCIATION, INC.
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Countertrue

Customer Support Contacts

Phone248-449-9300
Emailxx@xx.xx
Phone248-449-9300
Emailxx@xx.xx

Device Dimensions

Length5 Millimeter
Length5 Millimeter
Length5 Millimeter
Length5 Millimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 5 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 5 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100384703590004 [Unit of Use]
GS100635515959392 [Primary]
GS100761059591337 [Package]
Package: Sleeve [10 Units]
In Commercial Distribution
GS100761059592334 [Package]
Contains: 00761059591337
Package: Case [50 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 Number3
Public Version Date2018-07-06
Device Publish Date2016-09-19

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