GUDID 20650862199073

PATIENT TUBE PACK, NON-LATEX, 3/8

ATRIUM MEDICAL CORPORATION

Mediastinal drainage catheter Mediastinal drainage catheter Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial Mediastinal drainage catheter, non-antimicrobial
Primary Device ID20650862199073
NIH Device Record Key9db1d50b-fdae-4c23-b4c7-0cdb72c193a3
Commercial Distribution StatusIn Commercial Distribution
Version Model Number19907
Company DUNS051798999
Company NameATRIUM MEDICAL CORPORATION
Device Count1
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100650862199079 [Primary]
GS120650862199073 [Package]
Contains: 00650862199079
Package: [10 Units]
In Commercial Distribution

FDA Product Code

KDQBOTTLE, COLLECTION, VACUUM

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-01-15
Device Publish Date2015-09-24

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