FDA UDI In Commercial Distribution 🇺🇸 United States

ElectrodeCRF

DI: 00811746032299 · Model: CRF-U1020P · CAMBRIDGE INTERVENTIONAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ElectrodeCRF
Primary DI
00811746032299
Version / Model
CRF-U1020P
Catalog Number
CRF-U1020P
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
0e87e00a-8d0c-4799-8443-91408f6f222f

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
64233 Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar

Identifiers

Type ID
Package 10811746032296
Primary 00811746032299

Customer Contacts

Phone
781-221-5300

Premarket Submissions

Submission Number Supplement Number
K192715 000