Depth Gauge 1040.10.012

GUDID 00854515008316

Unique Surgical

Surgical depth gauge, reusable

• Primary Device ID: 00854515008316
• NIH Device Record Key: 7366e083-1779-4789-a511-d64f4a6fb893
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Depth Gauge
• Version Model Number: Flexible Shaft
• Catalog Number: 1040.10.012
• Company DUNS: 079820535
• Company Name: Unique Surgical
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 818-813-8527
• Email: info@UniqueSurgical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00854515008316 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00854515008316]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-01-13
• Device Publish Date: 2023-01-05

On-Brand Devices [Depth Gauge]

• 00854515008316: Flexible Shaft
• 00854515008958: Cartilage
• 00854515008880: Paperclip Handle
• 00854515008781: Cartilage, 20mm