Martinez Clamp KS-9999MCR

GUDID B033KS9999MCR0

Martinez Clamp – Right (7”)

Kapp Surgical Instrument Co.

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

• Primary Device ID: B033KS9999MCR0
• NIH Device Record Key: 414df230-cf87-40ba-8068-10ec81086459
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Martinez Clamp
• Version Model Number: KS-9999MCR
• Catalog Number: KS-9999MCR
• 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	B033KS9999MCR0 [Primary]

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

[B033KS9999MCR0]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-21
• Device Publish Date: 2023-06-13

On-Brand Devices [Martinez Clamp]

• B033KS9999MCR0: Martinez Clamp – Right (7”)
• B033KS9999MCL0: Martinez Clamp – Left (7”)