FDA UDI In Commercial Distribution 🇺🇸 United States

Cannulated Screw System +

DI: 00810040681936 · Model: 03.333.013S · Tyber Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cannulated Screw System +
Primary DI
00810040681936
Version / Model
03.333.013S
Catalog Number
03.333.013S
Company Name
Tyber Medical LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-21
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
c08b7902-e7b2-4cc1-b040-87abafa90e35

Device Description

1.6MM THREADED GUIDE WIRE 220MM LENGTH-STER

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary 00810040681936

Customer Contacts