FDA UDI Not in Commercial Distribution 🇺🇸 United States

LEVEL ONE CMF

DI: 10888118094589 · Model: 995-6458-02 · KLS-Martin L.P.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
LEVEL ONE CMF
Primary DI
10888118094589
Version / Model
995-6458-02
Company Name
KLS-Martin L.P.
Labeler DUNS
826499238
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-03-24
Public Version
8
Public Version Date
2023-11-10
Public Version Status
Update
Public Device Record Key
ab432c14-62dd-47c4-81b1-15288b470de6
Distribution End Date
2021-04-20

Device Description

SCREW, MAXDRIVE, F3, TI-6AL-4V

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
JEY PLATE, BONE

GMDN Terms

Code Name
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 10888118094589
Unit of Use 00888118094582

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1.5 X 5 MM