3M™ V.A.C.® EZ5SML

GUDID 50849554013860

3M™ V.A.C.® Peel and Place Dressing Kit, EZ5SML, Small, 5/CS

KCI USA, INC.

Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial Negative-pressure wound therapy system foam dressing, non-antimicrobial
Primary Device ID50849554013860
NIH Device Record Key6ef75ed2-1e58-4a96-b35a-76ba1f854bb6
Commercial Distribution StatusIn Commercial Distribution
Brand Name3M™ V.A.C.®
Version Model NumberEZ5SMLV001 / EZ5SMLV002
Catalog NumberEZ5SML
Company DUNS102726734
Company NameKCI USA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110849554013862 [Primary]
GS150849554013860 [Package]
Contains: 10849554013862
Package: BOX [5 Units]
In Commercial Distribution
GS150849554014997 [Package]
Contains: 10849554013862
Package: BOX [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OMPnegative pressure wound therapy Powered suction pump

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-13
Device Publish Date2024-03-05

On-Brand Devices [3M™ V.A.C.®]

508495540138843M™ V.A.C.® Peel and Place Dressing Kit, EZ5LRG, Large, 5/CS
508495540150003M™ V.A.C.® Peel and Place Dressing Kit, EZ5MED, Medium, 5/CS
508495540138603M™ V.A.C.® Peel and Place Dressing Kit, EZ5SML, Small, 5/CS

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