MEDIAFIT 10900MP

GUDID 04048551311202

MediaFIT Forceps Insert

Karl Storz GmbH & Co. KG

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

• Primary Device ID: 04048551311202
• NIH Device Record Key: 9ac543c3-5f65-46df-8be6-d7090bd5e00e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDIAFIT
• Version Model Number: 10900MP
• Catalog Number: 10900MP
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	04048551311202 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K940427

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

[04048551311202]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-08-01
• Device Publish Date: 2016-09-23

On-Brand Devices [MEDIAFIT]

• 04048551311202: MediaFIT Forceps Insert
• 04048551311196: MediaFIT Forceps Insert
• 04048551266144: MediaFIT Biopsy Forceps Insert
• 04048551266113: MediaFIT Forceps Insert