FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00885556805862 · Model: 74037032 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885556805862
Version / Model
74037032
Catalog Number
74037032
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-28
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
cef026b5-df86-47e8-b59c-e964e7524e19

Device Description

CEMENTED ROUND PATELLA W/ JRNY PEGS 9.0MM 32MM TRIAL

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
58714 Patella prosthesis trial

Identifiers

Type ID
Primary 00885556805862

Customer Contacts