FDA UDI In Commercial Distribution 🇺🇸 United States

ESTREMO FIBULAR NAIL

DI: 08059386742150 · Model: Estremo Fibular Nail guide · CITIEFFE SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ESTREMO FIBULAR NAIL
Primary DI
08059386742150
Version / Model
Estremo Fibular Nail guide
Catalog Number
FN900010
Company Name
CITIEFFE SRL
Labeler DUNS
431406875
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-19
Public Version
1
Public Version Date
2025-12-29
Public Version Status
New
Public Device Record Key
214896ed-a199-45d8-9a38-539b4f8ad8b2

Device Description

Estremo Fibular Nail - Guide

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
No
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
HSB Rod, Fixation, Intramedullary And Accessories

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 08059386742150

Customer Contacts

Phone
+39051721850

Premarket Submissions

Submission Number Supplement Number
K250197 000