FDA UDI Not in Commercial Distribution 🇺🇸 United States

ACCURIS

DI: 00885556057162 · Model: 71932132 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACCURIS
Primary DI
00885556057162
Version / Model
71932132
Catalog Number
71932132
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-28
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
544be08b-c04b-4704-94e6-a08fa3779e97
Distribution End Date
2016-07-03

Device Description

ACCURIS UNI TIBIAL INLAY TRIAL 34 X 7MM

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
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 00885556057162

Customer Contacts