FDA UDI In Commercial Distribution 🇺🇸 United States

LEONE SPA

DI: 08033707087366 · Model: 123-3300-01 · 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
08033707087366
Version / Model
123-3300-01
Catalog Number
123-3300-01
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
c714f622-4ac1-476d-98e9-81b9be74ce24

Device Description

BALL HEAD ABUTMENT IMP 3,3GH 1,5MM

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 08033707087366

Premarket Submissions

Submission Number Supplement Number
K050586 000