FDA UDI In Commercial Distribution 🇺🇸 United States

ELOS

DI: 08056693001420 · Model: 200.1095 · INTRAUMA SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELOS
Primary DI
08056693001420
Version / Model
200.1095
Catalog Number
200.1095
Company Name
INTRAUMA SPA
Labeler DUNS
387588051
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-12
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
53857cb0-aedc-4734-ad45-0272c8d4cd0f

Device Description

Cannulated Cephalic Screw

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HSB Rod, Fixation, Intramedullary And Accessories

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 08056693001420

Premarket Submissions

Submission Number Supplement Number
K201147 000

Device Sizes

Type Value Unit Text
Length 95 Millimeter
Device Size Text, specify Diameter: 10.5 Millimiter