IntePro Y-Mesh 72404000

GUDID 00814723020333

IntePro Y-Mesh

ENDO PHARMACEUTICALS INC.

Pelvic organ prolapse surgical mesh, synthetic polymer
Primary Device ID00814723020333
NIH Device Record Key627a14b5-452e-4152-a39e-5042f2f5d195
Commercial Distribution Discontinuation2016-03-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameIntePro Y-Mesh
Version Model Number72404000
Catalog Number72404000
Company DUNS178074951
Company NameENDO PHARMACEUTICALS 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18448790787
Emailcrabtree.tim@endo.com
Phone18448790787
Emailcrabtree.tim@endo.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store product in a clean, dry, dark area at room temperature.
Special Storage Condition, SpecifyBetween 0 and 0 *Store product in a clean, dry, dark area at room temperature.

Device Identifiers

Device Issuing AgencyDevice ID
GS100814723020333 [Primary]

FDA Product Code

OTOMesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-10-24

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