FDA UDI In Commercial Distribution 🇺🇸 United States

ROMEO Posterior Osteosynthesis System

DI: 07640178984585 · Model: ELL-PS 08 10-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
07640178984585
Version / Model
ELL-PS 08 10-S
Catalog Number
ELL-PS 08 10-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-04
Public Version
1
Public Version Date
2018-05-07
Public Version Status
New
Public Device Record Key
5fdd75c6-6e0e-4774-a9b1-12c299959d6b

Device Description

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

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

Identifiers

Type ID
Primary 07640178984585

Device Sizes

Type Value Unit Text
Outer Diameter 8 Millimeter
Length 100 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius