FDA UDI In Commercial Distribution 🇺🇸 United States

Comprehensive® Reverse Shoulder

DI: 00887868552090 · Model: 110031869 · Biomet Orthopedics, LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Comprehensive® Reverse Shoulder
Primary DI
00887868552090
Version / Model
110031869
Catalog Number
110031869
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-25
Public Version
3
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
8dddb42e-cbc4-4585-9c4a-636375315fe3

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
MBF PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED
PAO prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented
PHX shoulder prosthesis, reverse configuration

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00887868552090

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K172502 000