TiMESH

GUDID 04042301144324

Ti-Mesh 1.4" X 4" Light 35g/m²

pfm medical titanium gmbh

Abdominal hernia surgical mesh, synthetic polymer, non-bioabsorbable
Primary Device ID04042301144324
NIH Device Record Key7cc59412-1a12-4a9d-82d1-898029719c6b
Commercial Distribution StatusIn Commercial Distribution
Brand NameTiMESH
Version Model Number6000737
Company DUNS344675942
Company Namepfm medical titanium gmbh
Device Count1
DM Exemptfalse
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com
Phone7607588749
Emailregulatory@pfmmedicalusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104042301144317 [Primary]
GS104042301144324 [Package]
Contains: 04042301144317
Package: Box [3 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OXJMesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-17
Device Publish Date2019-12-09

On-Brand Devices [TiMESH]

04042301144348Ti-Mesh 1.4" X 4" Strong 65g/m²
04042301144324Ti-Mesh 1.4" X 4" Light 35g/m²
04042301097668Ti-Mesh 12" X 12" Light 35g/m²
04042301097651Ti-Mesh 6" X 8" Light 35g/m²
04042301097576Ti-Mesh 4" X 6" Light 35 g/m²
04042301097552Ti-Mesh 4" X 6" Extra Light 16 g/m²
04042301097606Ti-Mesh 6" X 6" Light 35g/m²

Trademark Results [TiMESH]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TIMESH
TIMESH
75315249 2220142 Dead/Cancelled
Sofamor Danek Properties, Inc.
1997-06-26
TIMESH
TIMESH
75102736 2047832 Live/Registered
MEDTRONIC, INC.
1996-05-13
TIMESH
TIMESH
73662837 1492999 Dead/Cancelled
TIMESH, INC.
1987-05-26

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