FDA UDI In Commercial Distribution 🇺🇸 United States

CannulaCRF

DI: 00811746030165 · Model: CRF-C2050 · CAMBRIDGE INTERVENTIONAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CannulaCRF
Primary DI
00811746030165
Version / Model
CRF-C2050
Catalog Number
CRF-C2050
Company Name
CAMBRIDGE INTERVENTIONAL LLC
Labeler DUNS
080897872
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-30
Public Version
2
Public Version Date
2023-09-27
Public Version Status
Update
Public Device Record Key
9cf7431d-c6c4-4e57-83a9-9b1610ff3e64

Device Description

CRF Radiofrequency Cannula

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
58739 Percutaneous radio-frequency ablation probe cannula, single-use

Identifiers

Type ID
Package 10811746030162
Primary 00811746030165

Customer Contacts

Phone
781-221-5300

Premarket Submissions

Submission Number Supplement Number
K192715 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius