Aspen® Rigid Light Handle Cover

GUDID 00840113201273

Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non-sterile) and the Surgeon or Nurse (sterile).

ASPEN SURGICAL PRODUCTS, INC.

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• Primary Device ID: 00840113201273
• NIH Device Record Key: c65feafb-cc67-451c-bc1a-8272e38a80c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aspen® Rigid Light Handle Cover
• Version Model Number: LT-R01
• 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	00840113201273 [Package]; Contains: 00840113201280; Package: [24 Units]; In Commercial Distribution
GS1	00840113201280 [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® Rigid Light Handle Cover]

• 10887761000145: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non
• 00887761000117: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non
• 00887761000025: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non
• 00840113201303: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non
• 00840113201273: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non
• 00840113201013: Single use, sterile. Provides a sterile interface between the operating room surgical lamps (non