VereSee

GUDID 00860012249954

VereSee, Camera Control Unit

Freyja Healthcare, LLC

Camera control unit

• Primary Device ID: 00860012249954
• NIH Device Record Key: dbd14cc8-dabb-4fad-8d73-e0eaaf1c121b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VereSee
• Version Model Number: VER-100-103
• Company DUNS: 117584088
• Company Name: Freyja Healthcare, LLC
• 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: false
• Lot Batch: false
• Serial Number: true
• 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

Customer Support Contacts

• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com
• Phone: 8333739521
• Email: CS@FreyjaHealthcare.com

Device Dimensions

• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound
• Weight: 3 Pound

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860012249954 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232464

FDA Product Code

• HIF: Insufflator, Laparoscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-26
• Device Publish Date: 2025-06-18

On-Brand Devices [VereSee]

• 00860012249916: VereSee, Optical Veres Needle, Single
• 00860012249954: VereSee, Camera Control Unit