FDA UDI In Commercial Distribution 🇺🇸 United States

Prometheus System Bone Screw

DI: 08806390897136 · Model: PRO-10210 · Jeil Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prometheus System Bone Screw
Primary DI
08806390897136
Version / Model
PRO-10210
Company Name
Jeil Medical Corporation
Labeler DUNS
688811603
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-01
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
c24c115a-0f8e-408d-8afc-835ae433c557

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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 08806390897136

Premarket Submissions

Submission Number Supplement Number
K171285 000
K180972 000
K193616 000