FDA UDI In Commercial Distribution 🇺🇸 United States

GENESIS II

DI: 03596010212993 · Model: 71430716 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GENESIS II
Primary DI
03596010212993
Version / Model
71430716
Catalog Number
71430716
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
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
5c9b69c8-ec25-4791-943c-1a8ccfde6855

Device Description

GNS II ANGLED HEMI TIB WEDGE TRIAL SZ3-4 20 DEGREE

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
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 03596010212993

Customer Contacts