FDA.reportPublic FDA data

Medifoam

Primary DI
08806129660031
Brand
Medifoam
Company
Genewel Co.,Ltd.
Model
12NL02
Device description
Medifoam is indicated for the management of exuding wounds such as ulcers, burns, surgical/traumatic/acute, lacerations, abrasions, etc. It readily absorbs exudate, providing a moist wound interface that produces an optimal wound healing environment. To help adhesion, a non-woven fabric for fixation is enclosed with the product. Medifoam is a sterile, but Non-woven fabric is a non-sterile. This is single-use product, do not re-use. This product does not include a hydrophilic wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.
Published
2022-10-30
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
NACDressing, Wound, Hydrophilic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NACDressing, Wound, HydrophilicGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08806129660031PrimaryGS10
08806129660093Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806129660031088061296600318806129660031
08806129660093088061296600938806129660093

GMDN Terms#

Term, Definition table
TermDefinition
Exudate-absorbent dressing, non-gel, non-antimicrobialA wound covering intended to assist in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) and often by creating a moist wound-healing environment. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudates, but may be designed to absorb and remove exudates (e.g., by capillary action); it does not contain an antimicrobial agent, but may include antioxidant properties. The device is available in a variety of forms (e.g., flat sheet/film-like, impregnated pouches, filled sachets, lyophilized matrix, ribbon, rope, foam, liquid, or powder). After application, this device cannot be reused.

Regulatory Flags#

DUNS number
987669599
Device count
3
Premarket exempt
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08806129660185Medifoam12NJ052025-03-03
08806129660208Medifoam bandMBD03401512025-03-03
08806129660222Medifoam H band MediumMB291303M2025-03-03
08806129660239Medifoam H band MediumMB291303M2025-03-03
08806129660253Medifoam H band largeMB352003L2025-03-03
08806129660260Medifoam H band largeMB352003L2025-03-03
08806129660178Medifoam12NJ052025-03-03
08806129660192Medifoam bandMBD03401512025-03-03
08806129660215Medifoam H band MediumMB291303M2025-03-03
08806129660246Medifoam H band largeMB352003L2025-03-03
08806129660109Medifoam HML100100032022-11-30
08806129660000Medifoam HML100100032022-10-30
08806129660147Medifoam H beautyMVmix12022-10-30
08806129660161Medifoam H bandMB2513032022-10-30
08806129660048Medifoam HML100100032022-10-30
08806129660093Medifoam12NL022022-10-30
08806129660055Medifoam H beautyMVmix12022-10-30
08806129660062Medifoam H bandMB2513032022-10-30

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Primary DI, Brand, Company table
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