FDA UDI In Commercial Distribution 🇺🇸 United States

Tornier Perform® Reversed Augmented Glenoid

DI: 00846832092086 · Model: DWJ513 · TORNIER, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Tornier Perform® Reversed Augmented Glenoid
Primary DI
00846832092086
Version / Model
DWJ513
Catalog Number
DWJ513
Company Name
TORNIER, INC.
Labeler DUNS
968990812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-10
Public Version
2
Public Version Date
2023-10-16
Public Version Status
Update
Public Device Record Key
1543f231-a228-4e0e-862a-a5441ea95dc3

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
PHX shoulder prosthesis, reverse configuration

GMDN Terms

Code Name
48091 Reverse shoulder prosthesis base plate

Identifiers

Type ID
Package 10846832062000
Primary 00846832092086

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 29 Millimeter