FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOFIX

DI: 18053800898697 · Model: 1 · ORTHOFIX SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOFIX
Primary DI
18053800898697
Version / Model
1
Catalog Number
154996
Company Name
ORTHOFIX SRL
Labeler DUNS
438793622
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-01
Public Version
1
Public Version Date
2020-07-09
Public Version Status
New
Public Device Record Key
8f1806be-d67d-4f93-ba32-c24d81b684c2

Device Description

JPS MODULAR BASE 3.5MM INSTRUMENT

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
Yes
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
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 18053800898697

Customer Contacts

Device Sizes

Type Value Unit Text
Width 31 Millimeter