FDA UDI In Commercial Distribution 🇺🇸 United States

VLP

DI: 00885556385142 · Model: 74423020N · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VLP
Primary DI
00885556385142
Version / Model
74423020N
Catalog Number
74423020N
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-28
Public Version
7
Public Version Date
2024-02-21
Public Version Status
Update
Public Device Record Key
b5d2ba2d-23a0-41c3-87d6-68fb7f7c9bc8

Device Description

VLP TITANIUM 3.0MM X 20MM OSTEOPENIA SCREW T7 FULLY THREADED NON-STERILE

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
MR Conditional
Direct Marking Exempt
Yes
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
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 00885556385142

Customer Contacts