VLIFT IS2017VLF

GUDID 07613327278606

SPECIALTY SCREW ADJUSTER

Stryker Corporation

General internal orthopaedic fixation system implantation kit

• Primary Device ID: 07613327278606
• NIH Device Record Key: c5b1a75a-4470-45e2-a644-8d82ee53e9e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VLIFT
• Version Model Number: IS2017VLF
• Catalog Number: IS2017VLF
• 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: false
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	07613327278606 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

[07613327278606]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-02
• Device Publish Date: 2020-09-24

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