FDA UDI Not in Commercial Distribution 🇺🇸 United States

Elevate

DI: 00814723020050 · Model: 720093-01 · ENDO PHARMACEUTICALS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Elevate
Primary DI
00814723020050
Version / Model
720093-01
Catalog Number
720093-01
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
cc34f926-5e45-4765-b894-4877471ab529
Distribution End Date
2016-03-31

Device Description

Elevate Anterior & Apical

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
OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed

GMDN Terms

Code Name
60842 Pelvic organ prolapse surgical mesh, synthetic polymer

Identifiers

Type ID
Primary 00814723020050

Customer Contacts

Phone
18448790787

Storage Conditions

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