Rongeur K7-1800

GUDID 00841668108475

KERRISON RONGEUR SIZE 0

KATENA PRODUCTS, INC.

Craniofacial rongeur, reusable

• Primary Device ID: 00841668108475
• NIH Device Record Key: f27f3669-7e48-4373-a351-b3ddc6d5f1f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rongeur
• Version Model Number: K7-1800
• Catalog Number: K7-1800
• 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 Dimensions

• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0
• Width: 3 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841668108475 [Primary]

FDA Product Code

• HNG: Rongeur, lachrymal sac

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 [Rongeur]

• 00841668108529: BEYER RONGEUR SINGLE ACTION
• 00841668108512: CITELLI RONGEUR SMALL
• 00841668108505: KERRISON RONGEUR SIZE 3
• 00841668108499: KERRISON RONGEUR SIZE 2
• 00841668108482: KERRISON RONGEUR SIZE 1
• 00841668108475: KERRISON RONGEUR SIZE 0