FDA UDI In Commercial Distribution 🇺🇸 United States

LARGE CANNULATED SCREWS

DI: 03596010121646 · Model: 410236 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LARGE CANNULATED SCREWS
Primary DI
03596010121646
Version / Model
410236
Catalog Number
410236
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-14
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
7f8bbfb9-fbd5-41e1-bcea-0c53c88a6d60

Device Description

GUIDE PIN 230MM X 2.4MM

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
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
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
62729 Orthopaedic guidewire, single-use

Identifiers

Type ID
Package 23596010121640
Primary 03596010121646

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123055 000