FDA UDI In Commercial Distribution 🇺🇸 United States

VELOX

DI: 00193082161865 · Model: 4020-07-45 · SPINECRAFT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VELOX
Primary DI
00193082161865
Version / Model
4020-07-45
Catalog Number
4020-07-45
Company Name
SPINECRAFT, LLC
Labeler DUNS
783908713
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-07
Public Version
1
Public Version Date
2023-07-17
Public Version Status
New
Public Device Record Key
065fa097-130e-4678-a189-fc468b2f3e38

Device Description

Inserter Drill Guide Sleeve, 4mm and 5mm

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
Yes
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
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00193082161865

Customer Contacts