FDA UDI In Commercial Distribution 🇺🇸 United States

R3

DI: 00885556653340 · Model: E0015118-1 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
R3
Primary DI
00885556653340
Version / Model
E0015118-1
Catalog Number
E0015118-1
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-13
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0b1d8b48-cc86-48d9-b56f-7e2a8e7b5578

Device Description

MODIFIED -3MM OFFSET TRIAL HEAD SZ32MM

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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
58479 Femoral head prosthesis trial

Identifiers

Type ID
Primary 00885556653340

Customer Contacts