Vacurect

GUDID 00861753000200

Vacurect vacuum erection device with 5 tension systems, 2 oz personal lubricant, storage pouch, user's guide, and 1 year warranty.

MAINSPRING MEDICAL, LLC

Penile vacuum device

• Primary Device ID: 00861753000200
• NIH Device Record Key: 8afe96ce-45f8-4231-95b4-73ed2a493953
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vacurect
• Version Model Number: Custom 1002
• Company DUNS: 133686100
• Company Name: MAINSPRING MEDICAL, 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: 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: 7064264145
• Email: info@mainspringmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00861753000200 [Primary]

FDA Product Code

• LKY: Device, External Penile Rigidity

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-09

On-Brand Devices [Vacurect]

• 00861753000217: Vacurect vacuum erection device with 10 tension systems, 4 oz personal lubricant, 4 oz flavored
• 00861753000200: Vacurect vacuum erection device with 5 tension systems, 2 oz personal lubricant, storage pouch,