FDA UDI In Commercial Distribution 🇺🇸 United States

REFLECTION

DI: 03596010000941 · Model: 71358005 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REFLECTION
Primary DI
03596010000941
Version / Model
71358005
Catalog Number
71358005
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
88322c6c-63fc-4452-b61e-f3bb344ef601

Device Description

REFLECTION ALL POLY XLPE 22MM INNER DIAMETER 52MM OUTER DIAMETER

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
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented

GMDN Terms

Code Name
34076 Polyethylene acetabulum prosthesis

Identifiers

Type ID
Primary 03596010000941

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K002747 000
K211176 000