ARCADIUS XP C ME520

GUDID 04046955214686

ARCADIUS XP C TRIAL./INSERTION TRAY TOP

AESCULAP IMPLANT SYSTEMS, LLC

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• Primary Device ID: 04046955214686
• NIH Device Record Key: 218f002f-3217-494b-b685-6c59ca53c8b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARCADIUS XP C
• Version Model Number: ME520
• Catalog Number: ME520
• Company DUNS: 622600992
• Company Name: AESCULAP IMPLANT SYSTEMS, LLC
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046955214686 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

[04046955214686]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-22
• Device Publish Date: 2024-01-14

On-Brand Devices [ARCADIUS XP C]

• 04046955196227: ARCADIUSXP C BALL JOINT DRILL
• 04046955171477: ARCADIUSXP C BALL JOINT AWL
• 04046955171484: ARCADIUS XP C HEXALOBE BALL JNT SCREWDRV
• 04046955214747: ARCADIUS XP C SCREW CADDY TRAY LID
• 04046955214730: ARCADIUS XP C SCREW CADDY TRAY BASE
• 04046955214723: ARCADIUS XP C SCREW CADDY LID
• 04046955214716: ARCADIUS XP C SCREW CADDY CASE
• 04046955214686: ARCADIUS XP C TRIAL./INSERTION TRAY TOP
• 04046955214655: ARCADIUS XP C TRIAL./INSERT.TRAY MIDDLE