FDA UDI In Commercial Distribution 🇺🇸 United States

OSCAR PRO

DI: 18053340341820 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OSCAR PRO
Primary DI
18053340341820
Version / Model
1
Catalog Number
99-O4EL09B06
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-18
Public Version
1
Public Version Date
2021-03-26
Public Version Status
New
Public Device Record Key
9d64c663-b2bb-41cf-8897-a2e217328572

Device Description

OSCAR PRO TITANIUM OSTEOTOME WEDGE TIP L90MM W6MM STERILE

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
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-tissue ultrasonic surgical system

Identifiers

Type ID
Primary 18053340341820

Customer Contacts

Device Sizes

Type Value Unit Text
Length 90 Millimeter
Width 6 Millimeter