FDA UDI In Commercial Distribution 🇺🇸 United States

ELLIPSE Lumbar posterior osteosynthesis system

DI: 07640139340986 · Model: ELL-RD 01 80-N · SpineArt SA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELLIPSE Lumbar posterior osteosynthesis system
Primary DI
07640139340986
Version / Model
ELL-RD 01 80-N
Catalog Number
ELL-RD 01 80-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-06
Public Version
1
Public Version Date
2018-09-06
Public Version Status
New
Public Device Record Key
d870a100-4f08-4b99-867b-a20f01a0014c

Device Description

Pre-Bent Rod

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
Yes
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
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

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

Identifiers

Type ID
Primary 07640139340986

Device Sizes

Type Value Unit Text
Outer Diameter 5.4 Millimeter
Length 180 Millimeter