ULTRAPRO COMFORT PLUG UPLUG403

GUDID 20705031228426

Partially Absorbable Hernia Repair Device

Johnson & Johnson International Inc.

Abdominal hernia surgical mesh, composite-polymer
Primary Device ID20705031228426
NIH Device Record Key389492b1-2a03-46b2-b8df-f9c53b18d3f6
Commercial Distribution StatusIn Commercial Distribution
Brand NameULTRAPRO COMFORT PLUG
Version Model NumberUPLUG403
Catalog NumberUPLUG403
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

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damaged
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS110705031228429 [Primary]
GS120705031228426 [Package]
Contains: 10705031228429
Package: BOX [3 Units]
In Commercial Distribution

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 Number2
Public Version Date2020-04-28
Device Publish Date2019-09-24

On-Brand Devices [ULTRAPRO COMFORT PLUG]

20705031228471Partially Absorbable Hernia Repair Device
20705031228457Partially Absorbable Hernia Repair Device
20705031228433Partially Absorbable Hernia Repair Device
20705031228426Partially Absorbable Hernia Repair Device
20705031233291Partially Absorbable Hernia Repair Device
20705031233277Partially Absorbable Hernia Repair Device
20705031233253Partially Absorbable Hernia Repair Device
20705031233246Partially Absorbable Hernia Repair Device
10705031233287Partially Absorbable Hernia Repair Device
10705031233263Partially Absorbable Hernia Repair Device
10705031228467Partially Absorbable Hernia Repair Device
10705031228443Partially Absorbable Hernia Repair Device

Trademark Results [ULTRAPRO COMFORT PLUG]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ULTRAPRO COMFORT PLUG
ULTRAPRO COMFORT PLUG
85817614 4700291 Live/Registered
JOHNSON & JOHNSON
2013-01-08

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