FDA UDI In Commercial Distribution 🇺🇸 United States

REFLECTION

DI: 03596010550064 · Model: 71323138 · 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
03596010550064
Version / Model
71323138
Catalog Number
71323138
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
10
Public Version Date
2025-10-02
Public Version Status
Update
Public Device Record Key
aae2621d-effd-438d-8aba-03a0885281eb

Device Description

REFLECTION CONSTRAINED LINER 0 DEGREE 32MM INNER DIAMETER 66-68MM OUTER DIAMETER SIZE J

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
MR Conditional
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
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer

GMDN Terms

Code Name
58480 Acetabulum prosthesis trial, prefabricated, reusable

Identifiers

Type ID
Primary 03596010550064

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033442 000
K211176 000

Storage Conditions

Type
Special Storage Condition, Specify