SupraNET (EU) 11x12 PMIEU2432.1

GUDID 00810050460712

Non-Adherent Wound Dressing Coated on One Side (EU Distribution)

Bio Med Sciences, Inc.

Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial
Primary Device ID00810050460712
NIH Device Record Key8e1de624-f8a1-4209-9a85-c8090209356d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSupraNET (EU) 11x12
Version Model NumberPMIEU2432.1
Catalog NumberPMIEU2432.1
Company DUNS364435974
Company NameBio Med Sciences, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com
Phone+1(610)530-3193
EmailBioMedCS@silon.com

Device Dimensions

Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter
Width11 Inch
Length12 Inch
Length30 Centimeter
Width28 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100810050460712 [Primary]

FDA Product Code

NABGauze / sponge,nonresorbable for external use

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-01-08
Device Publish Date2023-12-31

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