SupraNET (US) 11x12 PMI2432.1

GUDID 00810050460682

Non-Adherent Wound Dressing Coated on One Side (US 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 ID00810050460682
NIH Device Record Keyf9b82ee7-d9a1-4b77-a9fc-e3280ef6bff2
Commercial Distribution StatusIn Commercial Distribution
Brand NameSupraNET (US) 11x12
Version Model NumberPMI2432.1
Catalog NumberPMI2432.1
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

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
Width11 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100810050460682 [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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