SCANLAN® MEMORY Instruments 8008-420

GUDID 00846159019858

Mirror Instrument

SCANLAN INTERNATIONAL INC

Neurosurgical probe

• Primary Device ID: 00846159019858
• NIH Device Record Key: 173f198c-1f71-41ac-bd8b-5eec638dcb68
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCANLAN® MEMORY Instruments
• Version Model Number: 8008-420
• Catalog Number: 8008-420
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846159019858 [Primary]

FDA Product Code

• GZX: Instrument, Microsurgical

Sterilization

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

[00846159019858]

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: 2016-08-17

On-Brand Devices [SCANLAN® MEMORY Instruments]

• 00846159019858: Mirror Instrument
• 00846159032437: SCANLAN® Septal Hook Angled, 3 Prong Sharp, 10"/25.4 cm