Mepitel® Ag

GUDID 07323190019762

Mepitel Ag 20x30cm US

Mölnlycke Health Care AB

Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial Wound-nonadherent dressing, permeable, antimicrobial
Primary Device ID07323190019762
NIH Device Record Key8b800738-3e34-4c3e-9a69-4f6caca14968
Commercial Distribution StatusIn Commercial Distribution
Brand NameMepitel® Ag
Version Model Number392090
Company DUNS631770658
Company NameMölnlycke Health Care AB
Device Count1
DM Exempttrue
Pre-market Exemptfalse
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+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com
Phone+46737733775
Emailpedro.lopes@molnlycke.com

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Device Identifiers

Device Issuing AgencyDevice ID
GS107323190019762 [Package]
Contains: 07323190019779
Package: CASE [6 Units]
In Commercial Distribution
GS107323190019779 [Package]
Contains: 07323190019939
Package: PACK_OR_INNER_PACK [5 Units]
In Commercial Distribution
GS107323190019939 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRODressing, wound, drug

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-31
Device Publish Date2022-10-21

On-Brand Devices [Mepitel® Ag]

07323190019816Mepitel Ag 20x50cm US
07323190019762Mepitel Ag 20x30cm US
07323190019731Mepitel Ag 10x18 US
07323190019687Mepitel Ag 10x12cm US
07323190019656Mepitel Ag 7,5x10cm US
07323190019618Mepitel Ag 5x7,5cm US

Trademark Results [Mepitel]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MEPITEL
MEPITEL
73721142 1682605 Live/Registered
MOLNLYCKE AB
1988-04-05

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