SCANLAN® Instrumentation 9009-823-13

GUDID 00846159036039

Miller™ Periosteal Elevator Curved

SCANLAN INTERNATIONAL INC

Periosteal elevator, reusable

• Primary Device ID: 00846159036039
• NIH Device Record Key: f0c1b906-4c77-4a76-8484-6aa4e9ed7bec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCANLAN® Instrumentation
• Version Model Number: 9009-823-13
• Catalog Number: 9009-823-13
• Company DUNS: 023055619
• Company Name: SCANLAN INTERNATIONAL INC
• 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: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846159036039 [Primary]

FDA Product Code

• HTE: Elevator

Sterilization

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

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

[00846159036039]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-22
• Device Publish Date: 2024-04-12

On-Brand Devices [SCANLAN® Instrumentation]

• 00846159026801: SCANLAN® Septal Hook
• 00846159026764: SCANLAN® Septal Hook
• 00846159035643: SCANLAN® Cardiovascular Probe
• 00846159033656: Kerrison Style Wire Cutter
• 00846159035858: SCANLAN® Retractor Blade
• 00846159035841: SCANLAN® Retractor Blade
• 00846159035919: Suction Instrument
• 00846159036046: Miller™ Periosteal Elevator Curved
• 00846159036039: Miller™ Periosteal Elevator Curved