FDA UDI In Commercial Distribution 🇺🇸 United States

ELITE

DI: 03596010621344 · Model: 72202202 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELITE
Primary DI
03596010621344
Version / Model
72202202
Catalog Number
72202202
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
12
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
3eda7f58-71ae-42aa-8e4f-01705dfd023c

Device Description

ELITE PREMIUM BICEPS TENODESIS TRAY

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 03596010621344

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090562 000