RONDO' VP-13012

GUDID 08032909622191

Titanium cannulated screw ø3mm L12mm with washer. Material: titanium alloy Ti6Al4V ELI (ASTM F136).

CITIEFFE SRL

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 08032909622191
• NIH Device Record Key: 8fa184ab-2ae7-497b-9c27-d7f18fe0f3d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RONDO'
• Version Model Number: Screw ø3mm L12mm
• Catalog Number: VP-13012
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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

Device Dimensions

• Length: 12 Millimeter
• Outer Diameter: 3 Millimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Dry and clean environment and avoid damaging the packing. Room temperature.

Device Identifiers

Device Issuing Agency	Device ID
GS1	08032909622191 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113388

FDA Product Code

• HTY: Pin, Fixation, Smooth

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-02-19
• Device Publish Date: 2015-10-21