7.3mm Depth Gauge 6042

GUDID 00811954013028

INTERVENTIONAL SPINE, INC

Surgical depth gauge, reusable Surgical depth gauge, reusable

• Primary Device ID: 00811954013028
• NIH Device Record Key: 166d62a6-9cfc-4461-8537-f449add9cae9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 7.3mm Depth Gauge
• Version Model Number: 6042
• Catalog Number: 6042
• Company DUNS: 017663522
• Company Name: INTERVENTIONAL SPINE, 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: 800-497-0484
• Email: www.cs@i-spineinc.com
• Phone: 800-497-0484
• Email: www.cs@i-spineinc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811954013028 [Primary]

FDA Product Code

• HTJ: Gauge, Depth

Sterilization

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

[00811954013028]

Moist Heat or Steam Sterilization

[00811954013028]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-12-07
• Device Publish Date: 2015-12-22

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