FDA UDI In Commercial Distribution 🇺🇸 United States

EkoSonic®

DI: 00858593006264 · Model: 6795-002 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EkoSonic®
Primary DI
00858593006264
Version / Model
6795-002
Catalog Number
500-56112
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2021-06-22
Public Version Status
Update
Public Device Record Key
5ff91b7a-6d72-4a8d-97d1-bc6e8a2cd1c5

Device Description

The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRA Catheter, Continuous Flush

GMDN Terms

Code Name
59223 Ultrasound thrombolysis system catheter, pulmonary
59026 Ultrasound thrombolysis system catheter, peripheral

Identifiers

Type ID
Primary 00858593006264

Customer Contacts

Phone
888-400-3567

Device Sizes

Type Value Unit Text
Device Size Text, specify 12 cm TZ
Length 135 Centimeter