FDA UDI In Commercial Distribution 🇺🇸 United States

X-Mark Ultra

DI: EIBA10720 · Model: 1072 · Izi Medical Products, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
X-Mark Ultra
Primary DI
EIBA10720
Version / Model
1072
Catalog Number
1072
Company Name
Izi Medical Products, LLC
Labeler DUNS
933506164
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2023-09-22
Public Version Status
Update
Public Device Record Key
d3e590e0-ee71-4147-aab7-579e450fd4b8
Distribution End Date
2025-12-31

Device Description

0.85mm x 3cm X-MARK ULTRA Loose

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
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
40808 Radiological image marker, implantable

Identifiers

Type ID
Primary EIBA10720

Customer Contacts

Phone
9014327202