FDA UDI In Commercial Distribution 🇺🇸 United States

Cannulated Screw System +

DI: 00810040630644 · Model: 04.353.110 · Tyber Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cannulated Screw System +
Primary DI
00810040630644
Version / Model
04.353.110
Catalog Number
04.353.110
Company Name
Tyber Medical LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-08
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
a251bf32-8aed-4de7-b967-a3555a84cdcb

Device Description

2.5MM TI CANN SCREW + ST - 10MM

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
No
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00810040630644

Customer Contacts