FDA UDI Not in Commercial Distribution 🇺🇸 United States

REFLECTION

DI: 00885556020494 · Model: 71338346 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REFLECTION
Primary DI
00885556020494
Version / Model
71338346
Catalog Number
71338346
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-04
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
4b6624b1-6b8d-4cea-b2e2-da079a3e06a7
Distribution End Date
2022-03-17

Device Description

ALUMINA CERAMIC LINER 28ID 46-48OD

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
MRA Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

GMDN Terms

Code Name
48055 Ceramic acetabular liner

Identifiers

Type ID
Primary 00885556020494

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P030022 000