Vaxaid VX-V7-T

GUDID 05060140208518

Vaxaid V7 Trainer

DX PRODUCTS LIMITED

Penile vacuum device

• Primary Device ID: 05060140208518
• NIH Device Record Key: 674e414d-8ea4-49c6-8f0e-e0ae81ad4928
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vaxaid
• Version Model Number: Vaxaid V7 Trainer
• Catalog Number: VX-V7-T
• Company DUNS: 216732051
• Company Name: DX PRODUCTS LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com
• Phone: +4401924288094
• Email: tim@vaxaid.com

Device Dimensions

• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch
• Depth: 7 Inch
• Lumen/Inner Diameter: 2.1 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060140200932 [Package]; Contains: 05060140208501; Package: BOX [10 Units]; In Commercial Distribution
GS1	05060140208501 [Primary]
GS1	05060140208518 [Package]; Contains: 05060140208501; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• LKY: Device, External Penile Rigidity

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: 2019-03-11
• Device Publish Date: 2019-03-01

On-Brand Devices [Vaxaid]

• 05060140208532: Vaxaid V9 Delux
• 05060140208518: Vaxaid V7 Trainer
• 05060140208495: Vaxaid V7 Delux
• 05060140208471: Vaxaid V5 Trainer
• 05060140208457: Vaxaid V5 Delux
• 05060140208419: Vaxaid Peyronie's Disease
• 05060140200963: Vaxaid V3 Deluxe