NormaTec MVP Pro Full Body Recovery Package 40440

GUDID 00817369021825

MVP Pro Recovery Package - Full Body Standard

NORMATEC INDUSTRIES LP

Sequential venous compression system Sequential venous compression system Sequential venous compression system
Primary Device ID00817369021825
NIH Device Record Key913231b5-6936-475c-b8f2-f61223f57793
Commercial Distribution StatusIn Commercial Distribution
Brand NameNormaTec MVP Pro Full Body Recovery Package
Version Model NumberMVP Pro Recovery Package - Full Body Standard
Catalog Number40440
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100817369021825 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JOWSleeve, Limb, Compressible

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 Date2016-09-14

On-Brand Devices [NormaTec MVP Pro Full Body Recovery Package]

00817369021870MVP Pro Recovery Package - Full Body Power Tall
00817369021863MVP Pro Recovery Package - Full Body Power Standard
00817369021856MVP Pro Recovery Package - Full Body Power Short
00817369021849MVP Pro Recovery Package - Full Body Short
00817369021832MVP Pro Recovery Package - Full Body Tall
00817369021825MVP Pro Recovery Package - Full Body Standard

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