FDA UDI In Commercial Distribution 🇺🇸 United States

OSCAR PRO

DI: 18059015376111 · Model: 99-O4OL18B10 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OSCAR PRO
Primary DI
18059015376111
Version / Model
99-O4OL18B10
Catalog Number
99-O4OL18B10
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-14
Public Version
3
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
cb70d9c4-715f-46de-8c1c-26fc3405c4b9

Device Description

OSCAR PRO TITANIUM FLAT BLADE SMOOTH L180MM W10MM STERILE

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
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDX Instrument, surgical, sonic and accessory/attachment

GMDN Terms

Code Name
45981 Hard/soft-tissue ultrasonic surgical system

Identifiers

Type ID
Primary 18059015376111

Customer Contacts

Device Sizes

Type Value Unit Text
Length 180 Millimeter
Width 10 Millimeter