TORQUE DEVICE 22215

GUDID 28717648013298

Torque Device

ABBOTT VASCULAR INC.

Torque manipulation device

• Primary Device ID: 28717648013298
• NIH Device Record Key: 06c4cb1b-6214-40c7-88ec-a5f21f7c6160
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TORQUE DEVICE
• Version Model Number: 22215
• Catalog Number: 22215
• Company DUNS: 964569052
• Company Name: ABBOTT VASCULAR INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)227-9902
• Email: AV.CUSTOMERCARE@AV.ABBOTT.COM

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a dry, dark, cool place.

Device Identifiers

Device Issuing Agency	Device ID
GS1	08717648013294 [Primary]
GS1	28717648013298 [Package]; Contains: 08717648013294; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• DQX: WIRE, GUIDE, CATHETER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-23
• Device Publish Date: 2016-08-05

On-Brand Devices [TORQUE DEVICE]

• 28717648013922: .035 Torque Device
• 28717648013298: Torque Device