SupraNET (EU) 5x10 PMIEU2350.1

GUDID 00810050460705

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 ID00810050460705
NIH Device Record Keyb17c2333-7e0d-47b0-b35e-629aeb2aead9
Commercial Distribution StatusIn Commercial Distribution
Brand NameSupraNET (EU) 5x10
Version Model NumberPMIEU2350.1
Catalog NumberPMIEU2350.1
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

Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch
Length25 Centimeter
Length10 Inch
Width13 Centimeter
Width5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100810050460705 [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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