FDA UDI In Commercial Distribution 🇺🇸 United States

U.L.I.S.™

DI: 03663136028071 · Model: IS2-MR1030T · SPINEVISION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
U.L.I.S.™
Primary DI
03663136028071
Version / Model
IS2-MR1030T
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-18
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0dfed68b-75ee-438d-ac2a-58d95d514bd3

Device Description

Multi-Axial Reduction Screw ø 10,5 mm L 30 mm

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
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
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 03663136028071

Customer Contacts

Phone
+33153332525

Device Sizes

Type Value Unit Text
Outer Diameter 10.5 Millimeter