Duramesh

GUDID 10850008298124

DURAMESH™ 2 Mesh Suture: Small Needle – USA

Mesh Suture Inc.

Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament Polyolefin/fluoropolymer suture, multifilament
Primary Device ID10850008298124
NIH Device Record Key54b5e5f2-4a6a-49bc-8449-055037ae3295
Commercial Distribution StatusIn Commercial Distribution
Brand NameDuramesh
Version Model NumberMSI-500
Company DUNS116375032
Company NameMesh Suture Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com
Phone800-298-5468
Emailinfo@meshsuture.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850008298127 [Primary]
GS110850008298124 [Package]
Contains: 00850008298127
Package: Shrink wrap sleeve [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GAWSuture, Nonabsorbable, Synthetic, Polypropylene

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-08
Device Publish Date2023-08-31

On-Brand Devices [Duramesh]

10850008298131DURAMESH™ 2 Mesh Suture: Large Needle – USA
10850008298124DURAMESH™ 2 Mesh Suture: Small Needle – USA
10850008298117DURAMESH™ 1 Mesh Suture: Large Needle – USA
10850008298100DURAMESH™ 1 Mesh Suture: Small Needle – USA
10850008298094DURAMESH™ 0 Mesh Suture: Large Needle – USA
00850008298080DURAMESH™ 0 Mesh Suture: Small Needle – USA
00850008298073DURAMESH™ 2-0 Mesh Suture: Small Needle – USA

Trademark Results [Duramesh]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DURAMESH
DURAMESH
88415265 not registered Live/Pending
Advanced Suture, Inc.
2019-05-03
DURAMESH
DURAMESH
87766478 not registered Live/Pending
Boot Royalty Company, L.P.
2018-01-23
DURAMESH
DURAMESH
86223976 not registered Dead/Abandoned
KIMBERLY-CLARK WORLDWIDE, INC.
2014-03-18
DURAMESH
DURAMESH
78441586 3099121 Dead/Cancelled
SUKOL CORPORATION
2004-06-25
DURAMESH
DURAMESH
78333859 not registered Indifferent
SUKOL SCIENTIFIC, INC.
0000-00-00
DURAMESH
DURAMESH
77707825 3743308 Dead/Cancelled
Krueger International, Inc.
2009-04-06
DURAMESH
DURAMESH
77574592 3703163 Dead/Cancelled
Ball Fabrics, Inc.
2008-09-19
DURAMESH
DURAMESH
75578347 not registered Dead/Abandoned
Johns Manville International, Inc.
1998-10-23
DURAMESH
DURAMESH
72351087 0923273 Dead/Cancelled
ALBANY INTERNATIONAL CORP.
1970-02-11
DURAMESH
DURAMESH
72002143 0634626 Dead/Expired
L.O.F. GLASS FIBERS COMPANY
1956-02-06
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