FDA UDI In Commercial Distribution 🇺🇸 United States

BiDop 7 probe

DI: 00894912002784 · Model: ST10M5S8A · KOVEN TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BiDop 7 probe
Primary DI
00894912002784
Version / Model
ST10M5S8A
Catalog Number
ST10M5S8A
Company Name
KOVEN TECHNOLOGY, INC.
Labeler DUNS
069261402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-20
Public Version
2
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
3727884d-fb2b-4e17-8add-e06bfab9be07

Device Description

10 mhz straight cable Probe for Bidop 7

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
DPW Flowmeter, Blood, Cardiovascular

GMDN Terms

Code Name
36970 Noninvasive vascular ultrasound system probe

Identifiers

Type ID
Primary 00894912002784

Customer Contacts

Phone
314-542-2101

Premarket Submissions

Submission Number Supplement Number
K201114 000