Po-T-Vac V110

GUDID 00656535000901

POS-T-VAC INC

Penile vacuum device Penile vacuum device

• Primary Device ID: 00656535000901
• NIH Device Record Key: aabbcc4b-7400-48dc-a87c-1b514e996491
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Po-T-Vac
• Version Model Number: VT-1 Complete System
• Catalog Number: V110
• Company DUNS: 186548160
• Company Name: POS-T-VAC INC
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00656535000901 [Primary]

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: 2018-10-01
• Device Publish Date: 2018-08-31

Devices Manufactured by POS-T-VAC INC

• 00656535000949 - Pos-T-Vac: 2018-10-22
• 00656535000284 - Pos-T-Vac: 2018-10-01
• 00656535000437 - Pos-T-Vac: 2018-10-01
• 00656535000444 - Pos-T-Vac: 2018-10-01
• 00656535000451 - Pos-T-Vac: 2018-10-01
• 00656535000482 - Pos-T-Vac: 2018-10-01
• 00656535000499 - Pos-T-Vac: 2018-10-01
• 00656535000505 - Pos-T-Vac: 2018-10-01