BiDop 7 probe ST8M05S8C

GUDID 00894912002951

8 mhz curly cable Probe for Bidop 7

KOVEN TECHNOLOGY, INC.

Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe Noninvasive vascular ultrasound system probe

• Primary Device ID: 00894912002951
• NIH Device Record Key: 2adc9423-b892-4491-943f-1cf76530ddcd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BiDop 7 probe
• Version Model Number: ST8M05S8C
• Catalog Number: ST8M05S8C
• Company DUNS: 069261402
• Company Name: KOVEN TECHNOLOGY, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com
• Phone: 314-542-2101
• Email: info@koven.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00894912002951 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201114

FDA Product Code

• DPW: Flowmeter, Blood, Cardiovascular

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-01-28
• Device Publish Date: 2021-01-20

On-Brand Devices [BiDop 7 probe]

• 00894912002982: 10 mhz curly cable Probe for Bidop 7
• 00894912002951: 8 mhz curly cable Probe for Bidop 7
• 00894912002821: 5 mhz curly cable Probe for Bidop 7
• 00894912002814: 2 mhz curly cable Probe for Bidop 7
• 00894912002784: 10 mhz straight cable Probe for Bidop 7
• 00894912002760: 8 mhz straight cable Probe for Bidop 7
• 00894912002753: 5 mhz straight cable Probe for Bidop 7
• 00894912002692: PPG Probe for Bidop 7