FDA UDI In Commercial Distribution 🇺🇸 United States

EMPERION

DI: 03596010536822 · Model: 71291371 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EMPERION
Primary DI
03596010536822
Version / Model
71291371
Catalog Number
71291371
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
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
3d24d8eb-be8e-490b-86f6-cf87f75a3264

Device Description

EMPERION 13 STEM LONG REVISION POLISHED +0 R

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
38155 Press-fit femoral stem prosthesis

Identifiers

Type ID
Primary 03596010536822

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K042127 000