TITANIUM DEBAKEY AORTIC CLAMP

GUDID B09926000210

TITANIUM DEBAKEY AORTIC CLAMP CURVED

SONTEC INSTRUMENTS, INC.

Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable Surgical bulldog clamp, reusable

• Primary Device ID: B09926000210
• NIH Device Record Key: 669d9db8-73d1-4e39-8625-f4b56539ba61
• Commercial Distribution Discontinuation: 2018-06-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: TITANIUM DEBAKEY AORTIC CLAMP
• Version Model Number: 2600-021
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, 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: false
• 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: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM

Device Dimensions

• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch
• Length: 13.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B09926000210 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092544

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09926000210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-08-08

On-Brand Devices [TITANIUM DEBAKEY AORTIC CLAMP]

• B09926000190: TITANIUM DEBAKEY AORTIC CLAMP CURVED CURVED
• B09926000210: TITANIUM DEBAKEY AORTIC CLAMP CURVED
• B09926000170: TITANIUM DEBAKEY AORTIC CLAMP CURVED
• B09926000150: TITANIUM DEBAKEY AORTIC CLAMP CURVED