FDA UDI Not in Commercial Distribution 🇺🇸 United States

Cannulated Screws

DI: 03596010471710 · Model: 71116080 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cannulated Screws
Primary DI
03596010471710
Version / Model
71116080
Catalog Number
71116080
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-28
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
1fbe4c42-0ad0-4d31-b39f-6b884b1cd1b8
Distribution End Date
2018-02-01

Device Description

CALIBRATED GUIDE PIN 3.2 X 500MM

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
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
45200 Orthopaedic stereotactic surgery system

Identifiers

Type ID
Primary 03596010471710

Customer Contacts