FDA.reportPublic FDA data

Medifoam H band Medium

Primary DI
08806129660215
Brand
Medifoam H band Medium
Company
Genewel Co.,Ltd.
Model
MB291303M
Published
2025-03-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
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
08806129660222PrimaryGS10
08806129660239PrimaryGS10
08806129660215Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806129660222088061296602228806129660222
08806129660239088061296602398806129660239
08806129660215088061296602158806129660215

GMDN Terms#

Term, Definition table
TermDefinition
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobialA wound covering, typically made of a hydrocolloid, hydrofibre, chitosan or alginate (salts and acids extracted from seaweed), intended to produce a water-absorbent gel upon contact with wound exudate; it does not contain an antimicrobial agent. The device assists in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) for minimal wound maceration, allowing wound debridement, and creating a moist wound-healing environment. The device may be in the form of a flat sheet/film, ribbon, rope, foam, liquid, paste, or powder. After application, this device cannot be reused.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
987669599
Device count
9
DM exempt
false
Premarket exempt
true
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
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
08806129660246Medifoam H band largeMB352003L2025-03-03
08806129660109Medifoam HML100100032022-11-30
08806129660000Medifoam HML100100032022-10-30
08806129660031Medifoam12NL022022-10-30
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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00197998295850Solventum™ Kerracel™Solventum US LLCNAC2026-06-27
00197998295898Solventum™ Kerracel™Solventum US LLCNAC2026-06-27
00197998295942Solventum™ Kerracel™Solventum US LLCNAC2026-06-27
00810178889921ViveCareVIVE HEALTH LLCNAC2026-05-29
00810178889938ViveCareVIVE HEALTH LLCNAC2026-05-29
00810178889945ViveCareVIVE HEALTH LLCNAC2026-05-29
00850087488433CeeportCEEPORT INC.NAC2026-05-29
00850087488440CeeportCEEPORT INC.NAC2026-05-29
00850087488518CeeportCEEPORT INC.NAC2026-05-29
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09551031940038DODODOTSDODO VENTURES SDN. BHD.NAC2026-04-22
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09551031940144DODODOTSDODO VENTURES SDN. BHD.NAC2026-04-22
09551031940151DODODOTSDODO VENTURES SDN. BHD.NAC2026-04-22
09551031940168DODODOTSDODO VENTURES SDN. BHD.NAC2026-04-22