FDA UDI In Commercial Distribution 🇺🇸 United States

Oxford® Partial Knee System

DI: 00889024683808 · Model: 512211115 · Biomet Uk Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Oxford® Partial Knee System
Primary DI
00889024683808
Version / Model
512211115
Catalog Number
512211115
Company Name
Biomet Uk Ltd
Labeler DUNS
219322575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-09
Public Version
1
Public Version Date
2026-04-17
Public Version Status
New
Public Device Record Key
35db00d2-e178-49aa-a795-a2577847536c

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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00889024683808

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 115 Magnification