FDA UDI In Commercial Distribution 🇺🇸 United States

R3

DI: 00885556309391 · Model: 71332432 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
R3
Primary DI
00885556309391
Version / Model
71332432
Catalog Number
71332432
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-23
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0959b5c4-2be4-4dba-b285-986e70057178

Device Description

R3 ANTEVERTED LINER TRIAL 28MM X 52MM +4

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
58480 Acetabulum prosthesis trial, prefabricated, reusable

Identifiers

Type ID
Primary 00885556309391

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182535 000