TITANIUM BECK AORTIC CLAMP

GUDID B09926051300

TITANIUM BECK INFANT AORTIC CLAMP

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: B09926051300
• NIH Device Record Key: 015f4e48-9ae3-4b0c-863b-8e387820abb1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TITANIUM BECK AORTIC CLAMP
• Version Model Number: 2605-130
• 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: true
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 6.5 Inch
• Length: 6.5 Inch
• Length: 6.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896005143 [Primary]
HIBCC	B09926051300 [Previous]

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

[B09926051300]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09926051300]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09926051300]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-21
• Device Publish Date: 2018-08-20

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