FDA UDI In Commercial Distribution 🇺🇸 United States

ELEOS™

DI: B27800103000090 · Model: 001-03-00009 · ONKOS SURGICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELEOS™
Primary DI
B27800103000090
Version / Model
001-03-00009
Catalog Number
001-03-00009
Company Name
ONKOS SURGICAL, INC.
Labeler DUNS
080254074
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-20
Public Version
8
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
9c7309a3-f7ec-407c-bb50-8dc94eeb8c5d

Device Description

ELEOS™ INSTRUMENTATION TRAY, FEMORAL RESURFACING INSTRUMENTS, TRAY 9

Device Characteristics

Single Use
No
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
Yes
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary B27800103000090

Customer Contacts