FDA UDI In Commercial Distribution 🇺🇸 United States

Alliance

DI: 00889024681996 · Model: 110040339 · Zimmer, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Alliance
Primary DI
00889024681996
Version / Model
110040339
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-06
Public Version
1
Public Version Date
2025-08-14
Public Version Status
New
Public Device Record Key
9f22a256-746c-4e17-8319-2465c3ab1850

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
PHX Shoulder Prosthesis, Reverse Configuration
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00889024681996

Premarket Submissions

Submission Number Supplement Number
K233148 000
K241043 000