FDA UDI In Commercial Distribution 🇺🇸 United States

ANTHEM

DI: 00885556583807 · Model: 71422685 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANTHEM
Primary DI
00885556583807
Version / Model
71422685
Catalog Number
71422685
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-09
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a9bcaf71-f598-43cd-95dd-d237727e3057

Device Description

ANTHEM POSTERIOR STABILIZED HI-FLEX INSERT SIZE 7-8 18MM

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
46585 Tibial insert

Identifiers

Type ID
Primary 00885556583807

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K032295 000