FDA UDI In Commercial Distribution 🇺🇸 United States

REFLECTION

DI: 03596010460165 · Model: 71336368 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REFLECTION
Primary DI
03596010460165
Version / Model
71336368
Catalog Number
71336368
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
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
60f7993a-2086-43f6-92d3-79895c91e524

Device Description

REFLECTION SPIKED SHELL 68MM

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
MBL Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous

GMDN Terms

Code Name
43167 Acetabular shell

Identifiers

Type ID
Primary 03596010460165

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K960094 000