FDA UDI In Commercial Distribution 🇺🇸 United States

MOBIO™ Total Knee System

DI: 00843575107602 · Model: 8829220002 · B-ONE ORTHO, CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MOBIO™ Total Knee System
Primary DI
00843575107602
Version / Model
8829220002
Catalog Number
8829220002
Company Name
B-ONE ORTHO, CORP.
Labeler DUNS
081315444
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-18
Public Version
1
Public Version Date
2022-11-28
Public Version Status
New
Public Device Record Key
51d0d880-fcf1-4bee-9f6c-5538216d2f52

Device Description

Trial Tibial Keel Adapter, Size - HJ

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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 00843575107602