FDA UDI In Commercial Distribution 🇺🇸 United States

SLR-PLUS

DI: 07611996095678 · Model: 75017278 · Smith & Nephew, Inc.
Product Codes
4
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SLR-PLUS
Primary DI
07611996095678
Version / Model
75017278
Catalog Number
75017278
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-19
Public Version
8
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
09d1c63c-1a21-4dcb-9bfd-0446e5ca59e0

Device Description

SLR-PLUS TRIAL BROACH 10

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 07611996095678

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123598 000