FDA UDI In Commercial Distribution 🇺🇸 United States

REFLECTION

DI: 03596010474124 · Model: 71333307 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
REFLECTION
Primary DI
03596010474124
Version / Model
71333307
Catalog Number
71333307
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
2025-11-26
Public Version Status
Update
Public Device Record Key
bf8f60f8-7fbc-4303-8283-843015079c56

Device Description

REFLECTION XLPE 22MM INNER DIAMETER 20 DEGREE 62-64MM OUTER DIAMETER SIZE H

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
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 03596010474124

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K002747 000
K211176 000

Storage Conditions

Type
Special Storage Condition, Specify