FDA UDI In Commercial Distribution 🇺🇸 United States

US Medical Innovations

DI: B413XL1000CP0 · Model: XL-1000CP · US MEDICAL INNOVATIONS, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
US Medical Innovations
Primary DI
B413XL1000CP0
Version / Model
XL-1000CP
Catalog Number
XL-1000CP
Company Name
US MEDICAL INNOVATIONS, LLC
Labeler DUNS
961656951
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-24
Public Version
1
Public Version Date
2024-07-02
Public Version Status
New
Public Device Record Key
c79a26e6-475d-4fe0-9278-405f8de3c3c5

Device Description

Canady Helios Cold Plasma Ablation System

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OAB Low Energy Direct Current Thermal Ablation System
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary B413XL1000CP0

Premarket Submissions

Submission Number Supplement Number
K240297 000