VLIFT 48292215

GUDID 04546540557841

ENDCAP

Stryker Corporation

Metallic spinal fusion cage, non-sterile

• Primary Device ID: 04546540557841
• NIH Device Record Key: cd7442d2-00aa-4935-9672-af1f49582013
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VLIFT
• Version Model Number: 48292215
• Catalog Number: 48292215
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• 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: true
• 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

Device Dimensions

• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0
• Angle: 15 degree
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540557841 [Primary]

FDA Product Code

• MQP: SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Sterilization

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

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

[04546540557841]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-26
• Device Publish Date: 2015-09-14

On-Brand Devices [VLIFT]

• 04546540557872: CAGE
• 04546540557865: CAGE
• 04546540557858: CAGE
• 04546540557841: ENDCAP
• 04546540557834: EXTENSION
• 04546540557827: CAGE
• 04546540557810: CAGE
• 04546540557803: CAGE
• 04546540557797: EXTENSION
• 04546540557780: ENDCAP
• 04546540557773: ENDCAP
• 04546540557766: ENDCAP
• 04546540557759: ENDCAP
• 04546540557742: ENDCAP
• 04546540557735: ENDCAP
• 04546540557728: ENDCAP
• 04546540557711: ENDCAP
• 04546540557704: ENDCAP
• 07613327119404: CONTAINER
• 07613327279870: SPECIALTY DUAL SIDED TRIAL
• 07613327278927: SPECIALTY DUAL SIDED TRIAL
• 07613327278606: SPECIALTY SCREW ADJUSTER
• 07613327267051: ENDCAP REMOVER
• 07613327267020: INSIDE SHAFT
• 07613327266986: EXPANDER