FDA UDI In Commercial Distribution 🇺🇸 United States

GENESIS II

DI: 03596010472823 · Model: 71422004 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GENESIS II
Primary DI
03596010472823
Version / Model
71422004
Catalog Number
71422004
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
9
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
dc073b1e-508f-4a3e-9e7f-f5dae32b6d43

Device Description

GENESIS II PLUS 4MM TIBIAL OFFSET COUPLER WITH SLEEVE

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
47847 Orthopaedic implant-instrument extension adaptor, reusable

Identifiers

Type ID
Primary 03596010472823

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K951987 000