FDA UDI In Commercial Distribution 🇺🇸 United States

LEONE SPA

DI: 08033707087458 · Model: 123-4115-03 · LEONE SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LEONE SPA
Primary DI
08033707087458
Version / Model
123-4115-03
Catalog Number
123-4115-03
Company Name
LEONE SPA
Labeler DUNS
432167294
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-25
Public Version
5
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
5f4e6855-c2e3-44a2-a982-8a1939547aeb

Device Description

BALL HEAD ABUTMENT 15°IMP 4,1 GH 3MM

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
No
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
High-level Disinfectant

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 08033707087458

Premarket Submissions

Submission Number Supplement Number
K050586 000