FDA UDI In Commercial Distribution 🇺🇸 United States

U.L.I.S.™

DI: 03663136017112 · Model: U1 - R660HC · SPINEVISION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
U.L.I.S.™
Primary DI
03663136017112
Version / Model
U1 - R660HC
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
6b21b6ba-4a43-45cb-b4ab-fba6b3c45f7c

Device Description

Co-Cr Rigid Rod Ø6.0mm x 600mm

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
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

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

Identifiers

Type ID
Primary 03663136017112

Premarket Submissions

Submission Number Supplement Number
K133575 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 6.0 Milliimeters Length: 600 Milliimeters