V.A.C. DERMATAC™

Primary DI
00849554005198
Brand
V.A.C. DERMATAC™
Company
KCI USA, INC.
Model
V.A.C. DERMATAC™
Device description
V.A.C. DERMATAC™ DRAPE
Published
2019-03-30
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Safe
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
OMPNegative Pressure Wound Therapy Powered Suction Pump

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OMPNegative Pressure Wound Therapy Powered Suction PumpGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K181505000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K181505000V.A.C. DERMATAC DrapeKci USA, Inc.2019-03-28OMP

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00849554005198PackageGS110In Commercial Distribution
00849554005242PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00849554005198008495540051988495540051980849554005198
00849554005242008495540052428495540052420849554005242

GMDN Terms#

Term, Definition table
TermDefinition
Negative-pressure wound therapy system drapeA sheet of plastic material designed to be placed over a wound dressing (e.g. open-cell foam or medicated gauze) to create a complete occlusion over and around a wound during negative pressure wound therapy (NPWT). This film dressing is typically vapour permeable, waterproof, and has an adhesive backing or edges applied against the wound dressing and surrounding healthy skin to create an airtight seal; it may be impregnated/coated with a gel (e.g., silicone) to minimize risk of trauma upon removal. It has a central opening, or an opening is made in or under it, to enable placement of the drain allowing negative pressure to reach the wound through the dressing. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
102726734
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00849554005532SNAP™ STPAL2016-09-24
00849554005549SNAP™ STPALP2016-09-24
00849554005563SNAP™ STPASP2016-09-24
00849554005570SNAP™ STPAMP2016-09-24
00849554005587SNAP™ STPAS2016-09-24
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108495540138863M™ V.A.C.®EZ5LRGV001 / EZ5LRGV002EZ5LRG2024-03-05
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00197998032608Solventum US LLCM8275026/5M8275026/52025-07-29
00197998312267Solventum US LLCM8275026/5M8275026/52025-07-29
00197998028939Solventum US LLCABT1055ABT10552025-07-29
00197998028953Solventum US LLCABT1055ABT10552025-07-29
00197998032615Solventum US LLCM8275026/5M8275026/52025-07-29
00197998312274Solventum US LLCM8275026/5M8275026/52025-07-29
00197998028809Solventum US LLCSTPASSTPAS2025-07-23
00197998028816Solventum US LLCSTPAMPSTPAMP2025-07-23

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