IntePro Y-Mesh 72404000

GUDID 00814723020333

Pelvic organ prolapse surgical mesh, synthetic polymer

Primary Device ID	00814723020333
NIH Device Record Key	627a14b5-452e-4152-a39e-5042f2f5d195
Commercial Distribution Discontinuation	2016-03-31
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	IntePro Y-Mesh
Version Model Number	72404000
Catalog Number	72404000
Company DUNS	178074951
Company Name	ENDO PHARMACEUTICALS INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

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

Device Issuing Agency	Device ID
GS1	00814723020333 [Primary]

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

Steralize Prior To Use	false
Device Is Sterile	true