FDA UDI In Commercial Distribution 🇺🇸 United States

Hybrid Glenoid

DI: 00880304462489 · Model: 113954 · Biomet Orthopedics, LLC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hybrid Glenoid
Primary DI
00880304462489
Version / Model
113954
Catalog Number
113954
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
5
Public Version Date
2021-09-21
Public Version Status
Update
Public Device Record Key
ebb8619c-380e-4bbe-afe3-175d952f6b21

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
KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED
MBF PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED

GMDN Terms

Code Name
36259 Shoulder glenoid fossa prosthesis, prefabricated

Identifiers

Type ID
Primary 00880304462489

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify MEDIUM SIZE 4 MM