ULTRAPRO COMFORT PLUG UPLUG406

GUDID 20705031233246

Partially Absorbable Hernia Repair Device

Johnson & Johnson International Inc.

Abdominal hernia surgical mesh, composite-polymer Abdominal hernia surgical mesh, composite-polymer Abdominal hernia surgical mesh, composite-polymer
Primary Device ID20705031233246
NIH Device Record Keya44b2b3c-5ccc-479f-8a3d-3a4d984fb6a3
Commercial Distribution Discontinuation2020-05-22
Commercial Distribution StatusIn Commercial Distribution
Brand NameULTRAPRO COMFORT PLUG
Version Model NumberUPLUG406
Catalog NumberUPLUG406
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

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Storage Environment Temperature
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 and 86 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Storage Environment Temperature
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 and 86 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Storage Environment Temperature
Storage Environment TemperatureBetween 0 and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 and 86 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS110705031233249 [Primary]
GS110705031233249 [Primary]
GS110705031233249 [Primary]
GS120705031233246 [Package]
Contains: 10705031233249
Package: BOX [6 Units]
Discontinued: 2020-05-22
In Commercial Distribution
GS120705031233246 [Package]
Contains: 10705031233249
Package: BOX [6 Units]
Discontinued: 2020-05-22
In Commercial Distribution
GS120705031233246 [Package]
Contains: 10705031233249
Package: BOX [6 Units]
Discontinued: 2020-05-22
In Commercial Distribution

FDA Product Code

FTLMesh, surgical, polymeric
FTLMesh, surgical, polymeric
FTLMesh, surgical, polymeric

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-05-21
Device Publish Date2015-09-01

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

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