FDA UDI In Commercial Distribution 🇺🇸 United States

FlexiMarc™

DI: 00853730006015 · Model: FM-0.9-3-10-GG-18-20 · CORTEX MANUFACTURING INC.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FlexiMarc™
Primary DI
00853730006015
Version / Model
FM-0.9-3-10-GG-18-20
Company Name
CORTEX MANUFACTURING INC.
Labeler DUNS
832596816
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-24
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
f6c71fd5-3f1c-4555-8875-605c80c73b6b

Device Description

Implanted Marker in Needle

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
33069 Brachytherapy needle
40808 Radiological image marker, implantable

Identifiers

Type ID
Primary 00853730006015

Premarket Submissions

Submission Number Supplement Number
K100267 000