FDA UDI In Commercial Distribution 🇺🇸 United States

GENESIS II

DI: 03596010214386 · Model: 71440192 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GENESIS II
Primary DI
03596010214386
Version / Model
71440192
Catalog Number
71440192
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
7138dfc0-849b-4269-9e9f-ed44b69849a2

Device Description

GENESIS II TIBIAL BASEPLATE IMPACTOR

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
No
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
JDG Prosthesis, hip, femoral component, cemented, metal

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 03596010214386

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123598 000