PREVENA PLUS DUO™ PEEL & PLACE™

GUDID 00849554006751

Prevena Plus Duo System with Peel & Place Dressing- 13cm/20cm

KCI USA, INC.

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Primary Device ID00849554006751
NIH Device Record Key3bd90047-4fea-41ac-bf13-38657bc1d55d
Commercial Distribution StatusIn Commercial Distribution
Brand NamePREVENA PLUS DUO™ PEEL & PLACE™
Version Model NumberPRE3321US
Company DUNS102726734
Company NameKCI USA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100849554006751 [Primary]

FDA Product Code

OMPNegative Pressure Wound Therapy Powered Suction Pump

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-09-10
Device Publish Date2017-12-19

On-Brand Devices [PREVENA PLUS DUO™ PEEL & PLACE™]

00849554006751Prevena Plus Duo System with Peel & Place Dressing- 13cm/20cm
00849554006744Prevena Plus Duo System with Peel & Place Dressing- 20cm/20cm

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