FDA UDI In Commercial Distribution 🇺🇸 United States

ElectrodeCRF

DI: 00811746032091 · Model: CRF-U2020L · CAMBRIDGE INTERVENTIONAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ElectrodeCRF
Primary DI
00811746032091
Version / Model
CRF-U2020L
Catalog Number
CRF-U2020L
Company Name
CAMBRIDGE INTERVENTIONAL LLC
Labeler DUNS
080897872
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-16
Public Version
2
Public Version Date
2023-09-28
Public Version Status
Update
Public Device Record Key
bf06b2d2-b4d3-4ec9-9471-e4b9afe6eec3

Device Description

CRF Radiofrequency Electrode

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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
61933 Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

Identifiers

Type ID
Package 10811746032098
Primary 00811746032091

Customer Contacts

Phone
781-221-5300

Premarket Submissions

Submission Number Supplement Number
K192715 000