Baby Renal Clamp – Left KS-1001

GUDID B033KS10010

Baby Renal Clamp – Left

Kapp Surgical Instrument Co.

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

• Primary Device ID: B033KS10010
• NIH Device Record Key: b5caa0bd-32fa-4f1a-8dbf-2c85a2c522fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Baby Renal Clamp – Left
• Version Model Number: KS-1001
• Catalog Number: KS-1001
• 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: true
• 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	B033KS10010 [Primary]

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

[B033KS10010]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-15
• Device Publish Date: 2023-06-07

Devices Manufactured by Kapp Surgical Instrument Co.

• B033KS99911 - PCL Retractor: 2025-04-23 PCL Retractor
• B033KS9993L1 - Lateral Tibia Retractor - Left: 2025-04-23 Lateral Tibia Retractor - Left
• B033KS9993R1 - Lateral Tibia Retractor - Right: 2025-04-23 Lateral Tibia Retractor - Right
• B033KS99941 - Knee Retractor: 2025-04-03 Medial Knee Retractor
• B033KS400140 - Coned Heparin Needles: 2023-06-22 Coned Heparin Needles – Size 01 - 4in
• B033KS400170 - Coned Heparin Needles: 2023-06-22 Coned Heparin Needles – Size 01 - 7in
• B033KS400240 - Coned Heparin Needles: 2023-06-22 Coned Heparin Needles – Size 02 - 4in
• B033KS400270 - Coned Heparin Needles: 2023-06-22 Coned Heparin Needles – Size 02 - 7in