FDA UDI In Commercial Distribution 🇺🇸 United States

REFLECTION

DI: 00885556535103 · Model: 71331091 · 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
00885556535103
Version / Model
71331091
Catalog Number
71331091
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-03
Public Version
1
Public Version Date
2025-12-11
Public Version Status
New
Public Device Record Key
cbc4c37a-e298-414a-aeb2-93986b302f37

Device Description

REFLECTION XLPE 32MM INNER DIAMETER 20 DEGREE 62-64MM OUTER DIAMETER SIZE H ETO

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
48055 Ceramic acetabular liner

Identifiers

Type ID
Primary 00885556535103

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K002747 000