StabiliT TOUCH™ Syringe IN8VCF/A

GUDID 00884450357019

Merit Medical Systems, Inc.

Orthopaedic cement preparation/delivery kit

• Primary Device ID: 00884450357019
• NIH Device Record Key: e768df8b-7848-4ec3-bf2b-c6789af98ff6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: StabiliT TOUCH™ Syringe
• Version Model Number: 00884450357019
• Catalog Number: IN8VCF/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450357019 [Primary]

FDA Product Code

• OAR: Injector, vertebroplasty (does not contain cement)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-06-08
• Device Publish Date: 2018-05-08

On-Brand Devices [StabiliT TOUCH™ Syringe]

• 00884450357019: 00884450357019
• 10884450662141: 00884450662144