FDA UDI In Commercial Distribution 🇺🇸 United States

Distraction Screw Pre-Drill

DI: 10840199515766 · Model: 7331-40 · KOROS U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Distraction Screw Pre-Drill
Primary DI
10840199515766
Version / Model
7331-40
Catalog Number
7331-40
Company Name
KOROS U.S.A., INC.
Labeler DUNS
007928633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-31
Public Version
1
Public Version Date
2025-01-08
Public Version Status
New
Public Device Record Key
eea37cc1-2d64-4f68-903e-f4aa777a16be

Device Description

Anterior Lumbar Distraction Screw Pre-Drill 4.5mm

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
Yes
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
FZX Guide, Surgical, Instrument

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Direct Marking 00840199515769
Primary 10840199515766

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place at room temperature