FDA UDI In Commercial Distribution 🇺🇸 United States

Headed Screw System

DI: M695409453850 · Model: 409-45385 · Tyber Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Headed Screw System
Primary DI
M695409453850
Version / Model
409-45385
Catalog Number
409-45385
Company Name
Tyber Medical, LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-12
Public Version
3
Public Version Date
2025-08-15
Public Version Status
Update
Public Device Record Key
927ef358-67a5-4660-9e5c-37c4e8c3e25f

Device Description

Headed Cannulated Screw Long Ø4.5mm x 85mm

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
Yes
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary M695409453850
Previous M695409453851C