Ankeney Sternal Retractor K-9779

GUDID B033K97790

Custom Ankeney Blades

Kapp Surgical Instrument Co.

Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable

• Primary Device ID: B033K97790
• NIH Device Record Key: cff6db69-f2a0-43ff-a408-d3d706024eaa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ankeney Sternal Retractor
• Version Model Number: K-9779
• Catalog Number: K-9779
• 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: 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: (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	B033K97790 [Primary]

FDA Product Code

• GAD: Retractor

Sterilization

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

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

[B033K97790]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-19
• Device Publish Date: 2023-06-09

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