FDA UDI In Commercial Distribution 🇺🇸 United States

Modular Knee Impactor Head, Tibia

DI: 00819251024051 · Model: 2227.00.000 · TOTAL JOINT ORTHOPEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Modular Knee Impactor Head, Tibia
Primary DI
00819251024051
Version / Model
2227.00.000
Company Name
TOTAL JOINT ORTHOPEDICS, INC.
Labeler DUNS
078416717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-04
Public Version
5
Public Version Date
2026-02-09
Public Version Status
Update
Public Device Record Key
28a2c429-e99c-48a7-b743-56a9df7593d9

Device Description

Tibial Impactor Head

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWA Impactor

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 00819251024051

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
The Klassic Knee System should be stored in a clean, dry location at room temperature