Spud K2-4800

GUDID 00841668101247

WILLS EYE SPUD AND BURR

KATENA PRODUCTS, INC.

Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud Eye spud

• Primary Device ID: 00841668101247
• NIH Device Record Key: 2a258de2-0800-4bc2-b50d-426a37f684d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spud
• Version Model Number: K2-4800
• Catalog Number: K2-4800
• Company DUNS: 085668598
• Company Name: KATENA PRODUCTS, INC.
• 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: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: info@katena.com
• Phone: +1(973)989-1600
• Email: inquiries.corzaeye@corza.com
• Phone: +1(973)989-1600
• Email: inquiries.corzaeye@corza.com
• Phone: +1(973)989-1600
• Email: inquiries.corzaeye@corza.com
• Phone: +1(973)989-1600
• Email: inquiries.corzaeye@corza.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841668101247 [Primary]

FDA Product Code

• HOF: Burr, corneal, manual

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-22
• Device Publish Date: 2020-09-14

On-Brand Devices [Spud]

• 00841668101247: WILLS EYE SPUD AND BURR
• 00841668101230: SPUD AND GOUGE REVERSIBLE HANDLE
• 00841668101223: ELLIS FOREIGN BODY SPUD
• 00841668101216: FRANCIS FOREIGN BODY SPUD
• 00841668101209: GOLF CLUB FOREIGN BODY SPUD
• 00857365004293: Golf Club Foreign Body Spud