FDA UDI In Commercial Distribution 🇺🇸 United States

FAICO CMF System

DI: 00840192710239 · Model: MLPS-2.0-C-10.0-TI-SC · FAICO MEDICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FAICO CMF System
Primary DI
00840192710239
Version / Model
MLPS-2.0-C-10.0-TI-SC
Company Name
FAICO MEDICAL LLC
Labeler DUNS
081290972
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-22
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e9a6c2e8-f0dd-45ba-8e26-7e1303995028

Device Description

Low Profile Screw. CROSS HEAD. D.2.0x10mm - Self-Tapping

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
Yes
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

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00840192710239