ULTRAPRO ADVANCED UPA31515

GUDID 20705031237008

Macroporous Partially Absorbable Mesh

Johnson & Johnson International Inc.

Abdominal hernia surgical mesh, composite-polymer
Primary Device ID20705031237008
NIH Device Record Key7f600765-8978-4f49-8d13-04224e6530e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameULTRAPRO ADVANCED
Version Model NumberUPA31515
Catalog NumberUPA31515
Company DUNS372587696
Company NameJohnson & Johnson International Inc.
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

Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx
Phone+1(877)384-4266
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS110705031237001 [Primary]
GS120705031237008 [Package]
Contains: 10705031237001
Package: BOX [3 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FTLMesh, surgical, polymeric

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-10-21
Device Publish Date2016-03-08

On-Brand Devices [ULTRAPRO ADVANCED]

10705031237032Macroporous Partially Absorbable Mesh
20705031237022Macroporous Partially Absorbable Mesh
20705031237015Macroporous Partially Absorbable Mesh
20705031237008Macroporous Partially Absorbable Mesh
20705031236995Macroporous Partially Absorbable Mesh
10705031236981Macroporous Partially Absorbable Mesh
10705031236974Macroporous Partially Absorbable Mesh
10705031236967Macroporous Partially Absorbable Mesh
10705031236950Macroporous Partially Absorbable Mesh

Trademark Results [ULTRAPRO ADVANCED]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ULTRAPRO ADVANCED
ULTRAPRO ADVANCED
86363731 5023088 Live/Registered
Johnson & Johnson
2014-08-12

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.