Aliquot 2110-0530

GUDID 00808232001211

Directional Bone Tamp

Stryker Corporation

Spinal curette Spinal curette Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use Neurosurgical curette, single-use

• Primary Device ID: 00808232001211
• NIH Device Record Key: 2c4aed1b-6c60-4f47-a19d-9c4e61fb260e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aliquot
• Version Model Number: 2110-0530
• Catalog Number: 2110-0530
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• 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: 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(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com
• Phone: +1(610)640-1775
• Email: inst.stryker.cs@stryker.com

Device Dimensions

• Length: 6 Inch
• Length: 6 Inch
• Length: 6 Inch
• Length: 6 Inch
• Needle Gauge: 14 Gauge
• Length: 6 Inch
• Needle Gauge: 14 Gauge
• Length: 6 Inch
• Needle Gauge: 14 Gauge
• Length: 6 Inch
• Needle Gauge: 14 Gauge
• Length: 6 Inch
• Needle Gauge: 14 Gauge
• Length: 6 Inch
• Needle Gauge: 14 Gauge
• Length: 6 Inch

Operating and Storage Conditions

• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00808232001211 [Primary]

FDA Product Code

• OCJ: spinal channeling instrument, vertebroplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-12-20

On-Brand Devices [Aliquot]

• 00808232001228: Directional Bone Tamp
• 00808232001211: Directional Bone Tamp
• 00808232001150: Side-Port Syringe
• 00808232001068: Plunger Delivery Kit
• 00808232001051: Syringe Delivery Kit
• 00808232001037: Plunger Delivery Kit
• 00808232001020: Syringe Delivery Kit
• 30808232001137: Flexible Extensions