Duffel Bag 30300

GUDID 00817369020668

Duffel Bag

NORMATEC INDUSTRIES LP

Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system
Primary Device ID00817369020668
NIH Device Record Keyeec4e268-75ea-4997-89f5-ade0fa891127
Commercial Distribution StatusIn Commercial Distribution
Brand NameDuffel Bag
Version Model NumberDuffel Bag
Catalog Number30300
Company DUNS111448069
Company NameNORMATEC INDUSTRIES LP
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100817369020668 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IRPMassager, Powered Inflatable Tube

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-22

Devices Manufactured by NORMATEC INDUSTRIES LP

00810050281294 - NormaTec2023-06-26
00810050281720 - NormaTec2023-06-26
00810050281768 - NormaTec 2023-06-26
00810050281782 - NormaTec2023-06-26
00810050281805 - NormaTec2023-06-26
00810050281829 - NormaTec2023-06-26
00810050281836 - NormaTec2023-06-26
00810050281881 - NormaTec2023-06-26

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