FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00885556022382 · Model: 71354015 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885556022382
Version / Model
71354015
Catalog Number
71354015
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a809f8c0-e01a-4a68-a39c-2648bffe55d4
Distribution End Date
2018-05-18

Device Description

MDF REVISION IMPLANT 300MM SZ 11

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
MEH Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

GMDN Terms

Code Name
34190 Uncoated hip femur prosthesis, modular

Identifiers

Type ID
Primary 00885556022382

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081124 000