VereSee

GUDID 00860012249916

VereSee, Optical Veres Needle, Single

Freyja Healthcare, LLC

Laparoscopic access cannula, single-use

• Primary Device ID: 00860012249916
• NIH Device Record Key: 478126fc-9640-4b83-aabc-3f7d770327f6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VereSee
• Version Model Number: VER-100-102
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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: 833.3739521
• Email: cs@FreyjaHealthcare.com
• Phone: 833.3739521
• Email: cs@FreyjaHealthcare.com
• Phone: 833.3739521
• Email: cs@FreyjaHealthcare.com
• Phone: 833.3739521
• Email: cs@FreyjaHealthcare.com
• Phone: 833.3739521
• Email: cs@FreyjaHealthcare.com
• Phone: 833.3739521
• Email: cs@FreyjaHealthcare.com
• Phone: 833.3739521
• Email: cs@FreyjaHealthcare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860012249916 [Primary]
GS1	00860012249947 [Package]; Package: Carton [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232464

FDA Product Code

• HIF: Insufflator, Laparoscopic

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: 2025-06-24
• Device Publish Date: 2025-06-16