Pulse Recovery Package 40104

GUDID 00817369020910

Pulse Recovery Package - Power Standard

NORMATEC INDUSTRIES LP

Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system
Primary Device ID00817369020910
NIH Device Record Keyd11e6d8d-0597-4e58-84b2-b5d1b92435e1
Commercial Distribution StatusIn Commercial Distribution
Brand NamePulse Recovery Package
Version Model NumberPulse Recovery Package - Power Standard
Catalog Number40104
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
GS100817369020910 [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 Recovery Package]

00817369020927Pulse Recovery Package - Power Tall
00817369020910Pulse Recovery Package - Power Standard
00817369020903Pulse Recovery Package - Power Short
00817369020897Pulse Recovery Package - Short
00817369020880Pulse Recovery Package - Tall
00817369020873Pulse Recovery Package - Standard

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