NormaTec MVP Pro Lower Body Recovery Package 40422

GUDID 00817369021726

MVP Pro Recovery Package - Lower Body Short

NORMATEC INDUSTRIES LP

Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system
Primary Device ID00817369021726
NIH Device Record Key1cfac993-4d2e-4e32-aa56-c627b9f06c0a
Commercial Distribution StatusIn Commercial Distribution
Brand NameNormaTec MVP Pro Lower Body Recovery Package
Version Model NumberMVP Pro Recovery Package - Lower Body Short
Catalog Number40422
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
GS100817369021726 [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 Lower Body Recovery Package]

00817369021757MVP Pro Recovery Package - Lower Body Power Tall
00817369021740MVP Pro Recovery Package - Lower Body Power Standard
00817369021733MVP Pro Recovery Package - Lower Body Power Short
00817369021726MVP Pro Recovery Package - Lower Body Short
00817369021719MVP Pro Recovery Package - Lower Body Tall
00817369021702MVP Pro Recovery Package - Lower Body Standard

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.