RONDO' VP-92203

GUDID 08056711928623

CITIEFFE SRL

Bone holding forceps

• Primary Device ID: 08056711928623
• NIH Device Record Key: 92be4822-7533-48a8-931e-2c4c5d7fd68d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RONDO'
• Version Model Number: Bone holding forceps, self-centering
• Catalog Number: VP-92203
• Company DUNS: 431406875
• Company Name: CITIEFFE SRL
• 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: true
• 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: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com
• Phone: +39051721850
• Email: info@citieffe.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056711928623 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113388

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

[08056711928623]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-22
• Device Publish Date: 2023-11-14