Pulse Pro Lower Body Recovery Package 40221

GUDID 00817369021214

Pulse Pro Recovery Package - Lower Body Tall

NORMATEC INDUSTRIES LP

Sequential venous compression system Sequential venous compression system Sequential venous compression system
Primary Device ID00817369021214
NIH Device Record Key177f3e49-adb1-40b2-a093-2ab387112b4f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePulse Pro Lower Body Recovery Package
Version Model NumberPulse Pro Recovery Package - Lower Body Tall
Catalog Number40221
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 Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100817369021214 [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 Date2016-09-13

On-Brand Devices [Pulse Pro Lower Body Recovery Package]

00817369021252Pulse Pro Recovery Package - Lower Body Power Tall
00817369021245Pulse Pro Recovery Package - Lower Body Power Standard
00817369021238Pulse Pro Recovery Package - Lower Body Power Short
00817369021221Pulse Pro Recovery Package - Lower Body Short
00817369021214Pulse Pro Recovery Package - Lower Body Tall
00817369021207Pulse Pro Recovery Package - Lower Body Standard

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