Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5m

GUDID 07640159550112

Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.50mm

Lanterna Medical Technologies GmbH

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 07640159550112
• NIH Device Record Key: 321849b3-d1fb-4989-966d-2f4be9558e1e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5m
• Version Model Number: 501-6550
• Company DUNS: 486405637
• Company Name: Lanterna Medical Technologies GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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: +41712800930
• Email: info@lanternamedtech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640159550112 [Primary]

FDA Product Code

• MNH: Orthosis, Spondylolisthesis Spinal Fixation

Sterilization

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

[07640159550112]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-09-03

On-Brand Devices [Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5m]

• 07640159550129: Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.55mm
• 07640159550112: Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.50mm
• 07640159550105: Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.45mm
• 07640159550099: Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.40mm
• 07640159550082: Santis Cannulated Polyaxial Pedicle Screw/Dia.6.5mm/Lng.35mm