Loop Aorta Clamp KS-7700

GUDID B033KS77000

Loop Aorta Clamp

Kapp Surgical Instrument Co.

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

• Primary Device ID: B033KS77000
• NIH Device Record Key: 27d74ae9-e8fe-46a2-849f-2d2abf0954ed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Loop Aorta Clamp
• Version Model Number: KS-7700
• Catalog Number: KS-7700
• Company DUNS: 004171112
• Company Name: Kapp Surgical Instrument Co.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com
• Phone: 216-587-4400
• Email: info@kappsurgical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B033KS77000 [Primary]

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

[B033KS77000]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-22
• Device Publish Date: 2023-06-14

On-Brand Devices [Loop Aorta Clamp]

• B033KS7700XL0: Loop Aorta Clamp – Extra Long
• B033KS77000: Loop Aorta Clamp