FDA UDI In Commercial Distribution 🇺🇸 United States

GLOBAL

DI: 10603295007005 · Model: 1136-43-025 · DEPUY ORTHOPAEDICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GLOBAL
Primary DI
10603295007005
Version / Model
1136-43-025
Catalog Number
113643025
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2019-12-23
Public Version Status
Update
Public Device Record Key
9708a16f-9a79-4d83-bc31-adada1859d42

Device Description

GLOBAL ANCHOR PEG GLENOID SIZE 52mm CEMENTED

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
No
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
KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
36259 Shoulder glenoid fossa prosthesis, prefabricated

Identifiers

Type ID
Primary 10603295007005

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K905786 000
K981487 000