FDA UDI In Commercial Distribution 🇺🇸 United States

TRIALTIS

DI: 10705034587813 · Model: 5560-63-5060S · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRIALTIS
Primary DI
10705034587813
Version / Model
5560-63-5060S
Catalog Number
5560635060S
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-17
Public Version
1
Public Version Date
2025-07-25
Public Version Status
New
Public Device Record Key
3155e6e8-1c5a-4a2d-9313-d14de343359b

Device Description

TRIALTIS Spine System Open Lateral Connector Fixed ø5.5-6mm to 5.5mm x 60mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
65114 Bone-screw internal spinal fixation system connector

Identifiers

Type ID
Primary 10705034587813

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K243249 000