V.A.C.VIA™

GUDID 00849554003750

VAC VIA 250ml Canister

KCI USA, INC.

Negative-pressure wound therapy system canister
Primary Device ID00849554003750
NIH Device Record Keyc37ac78b-964a-4b1e-b27d-2f4126c5964e
Commercial Distribution StatusIn Commercial Distribution
Brand NameV.A.C.VIA™
Version Model NumberVIACAN05
Company DUNS102726734
Company NameKCI USA, INC.
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 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
GS100849554002289 [Package]
Package: 5 Pack [5 Units]
In Commercial Distribution
GS100849554003750 [Primary]

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 StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-08-20
Device Publish Date2016-09-05

On-Brand Devices [V.A.C.VIA™ ]

00849554003750VAC VIA 250ml Canister
00849554003156VAC Via System Starter Kit
00849554002388VAC Via System 7-Day Kit

Trademark Results [V.A.C.VIA]

Mark Image

Registration | Serial
Company
Trademark
Application Date
V.A.C.VIA
V.A.C.VIA
77846707 3887702 Live/Registered
KCI Licensing, Inc.
2009-10-12

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