FDA UDI In Commercial Distribution 🇺🇸 United States

Leforte System Bone Screw

DI: 08809265152088 · Model: 20-MN-016 · Jeil Medical Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Leforte System Bone Screw
Primary DI
08809265152088
Version / Model
20-MN-016
Company Name
Jeil Medical Corporation
Labeler DUNS
688811603
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
e405022b-711d-4592-9d2d-06a24ca06cd6

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
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
DZL Screw, Fixation, Intraosseous
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 08809265152088

Premarket Submissions

Submission Number Supplement Number
K023365 000
K050669 000
K091686 000