Aspen® ALC Plus Light Handle Cover

GUDID 00840113201419

Intent ot use provides a sterile interface between the operating room surgical lamps (non-sterile) and the Surgeon or staff working in the sterile field.

ASPEN SURGICAL PRODUCTS, INC.

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• Primary Device ID: 00840113201419
• NIH Device Record Key: 476312fb-a46d-4a9a-b86a-6741ab39b05d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aspen® ALC Plus Light Handle Cover
• Version Model Number: LT-ALC01
• Company DUNS: 027680821
• Company Name: ASPEN SURGICAL PRODUCTS, INC.
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com
• Phone: +1(616)698-7100
• Email: customerservice@aspensurgical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840113201419 [Package]; Contains: 00840113201426; Package: [18 Units]; In Commercial Distribution
GS1	00840113201426 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020304

FDA Product Code

• FTA: Light, surgical, accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-05
• Device Publish Date: 2021-02-25

On-Brand Devices [Aspen® ALC Plus Light Handle Cover]

• 00887761000131: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non
• 10887761000121: Intent ot use provides a sterile interface between the operating room surgical lamps (non-steril
• 00840113201419: Intent ot use provides a sterile interface between the operating room surgical lamps (non-steril
• 00840113201402: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non