RHINOFORCE 459031

GUDID 04048551164594

RHINOFORCE® II Antrum Punch

Karl Storz GmbH & Co. KG

ENT soft-tissue cutting forceps

• Primary Device ID: 04048551164594
• NIH Device Record Key: 24fbef4b-4cc0-465d-af20-008e8652e913
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RHINOFORCE
• Version Model Number: 459031
• Catalog Number: 459031
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• 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: 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: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com
• Phone: +14242188201
• Email: regulatory@karlstorz.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048551164594 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

[04048551164594]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-08-01
• Device Publish Date: 2018-09-04

On-Brand Devices [RHINOFORCE]

• 04048551106761: Nasal Forceps, 45°, 1.5 mm, 18 cm
• 04048551106754: Forceps,through-cut, 1.5 mm, 25/45°
• 04048551106730: Nasal Forceps, 45°, 1.5 mm, 18 cm
• 04048551106723: Nasal Forceps, 1.5 mm, 18 cm
• 04048551235133: RHINOFORCE II Suction Punch, size 2
• 04048551205068: RHINOFORCE II Suction Punch, size 1
• 04048551164693: OSTRUM Antrum Punch, diameter 7 mm
• 04048551164655: PARSONS Punch, diameter 2.5 mm
• 04048551164648: PARSONS Punch, diameter 2.5 mm
• 04048551164631: PARSONS Punch, diameter 2.5 mm
• 04048551164600: RHINOFORCE® II Antrum Punch
• 04048551164594: RHINOFORCE® II Antrum Punch
• 04048551164587: RHINOFORCE® II Antrum Punch
• 04048551164570: Antrum Punch, 10 cm
• 04048551164556: RHINOFORCE® II Antrum Punch
• 04048551164549: RHINOFORCE®II Antrum Punch
• 04048551164532: RHINOFORCE® II Antrum Punch