SCANLAN® Retractor 1001-10-01

GUDID 00846159025682

SCANLAN® Retractor

SCANLAN INTERNATIONAL INC

Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00846159025682
• NIH Device Record Key: a712679c-c702-49e5-8a12-469f357b5bd4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCANLAN® Retractor
• Version Model Number: 1001-10-01
• Catalog Number: 1001-10-01
• 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	00846159025682 [Primary]

FDA Product Code

• GAD: Retractor

Sterilization

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

[00846159025682]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-16
• Device Publish Date: 2019-05-08

On-Brand Devices [SCANLAN® Retractor]

• 00846159025682: SCANLAN® Retractor
• 00846159031416: SCANLAN® Retractor