FDA UDI In Commercial Distribution 🇺🇸 United States

Genesis II

DI: 00885556491867 · Model: 71935032 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genesis II
Primary DI
00885556491867
Version / Model
71935032
Catalog Number
71935032
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a0747d29-12d7-4456-a2d9-79ccd8181002

Device Description

GENESIS II SWIVEL PATELLAR CEMENT CLAMP

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
HXD CLAMP

GMDN Terms

Code Name
34949 Bone approximation clamp

Identifiers

Type ID
Primary 00885556491867

Customer Contacts