SOLIS IS2421AVS

GUDID 07613327141924

SPECIALTY AS INSERTER WITH STOP

Stryker Corporation

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 07613327141924
• NIH Device Record Key: 03a537ec-206f-4898-b389-c74e8c2203f0
• Commercial Distribution Discontinuation: 2024-07-04
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOLIS
• Version Model Number: IS2421AVS
• Catalog Number: IS2421AVS
• 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	07613327141924 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

[07613327141924]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-06-28
• Device Publish Date: 2019-11-22

On-Brand Devices [SOLIS]

• 07613327262186: PIN GUIDE
• 07613327262131: DISTRACTION PIN
• 07613327262117: DISTRACTION PIN
• 07613327262063: PIN DRIVER
• 07613327141924: SPECIALTY AS INSERTER WITH STOP
• 07613327141870: SPECIALTY INSERTER WITH STOP