FDA UDI Not in Commercial Distribution 🇺🇸 United States

IntePro Y-Mesh

DI: 00814723020333 · Model: 72404000 · ENDO PHARMACEUTICALS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IntePro Y-Mesh
Primary DI
00814723020333
Version / Model
72404000
Catalog Number
72404000
Company Name
ENDO PHARMACEUTICALS INC.
Labeler DUNS
178074951
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
627a14b5-452e-4152-a39e-5042f2f5d195
Distribution End Date
2016-03-31

Device Description

IntePro Y-Mesh

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
60842 Pelvic organ prolapse surgical mesh, synthetic polymer

Identifiers

Type ID
Primary 00814723020333

Customer Contacts

Phone
18448790787

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store product in a clean, dry, dark area at room temperature.