FDA UDI In Commercial Distribution 🇺🇸 United States

ROMEO Posterior Osteosynthesis system

DI: 07640139344441 · Model: ELL-MS 07 80-S · SpineArt SA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROMEO Posterior Osteosynthesis system
Primary DI
07640139344441
Version / Model
ELL-MS 07 80-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-21
Public Version
5
Public Version Date
2019-02-13
Public Version Status
Update
Public Device Record Key
c17acf64-b05e-4cc6-b0cd-42bc8cbf9372

Device Description

Monoaxial Screw

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 07640139344441

Device Sizes

Type Value Unit Text
Length 80 Millimeter
Outer Diameter 7 Millimeter