ProV-Access Vascular Access Needle Guide Kit 5432

GUDID 10841912104694

PROTEK MEDICAL PRODUCTS, INC.

Nonimplantable needle guide, single-use

• Primary Device ID: 10841912104694
• NIH Device Record Key: d8fac4e8-ffd0-4ac3-bd48-02d7685558d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProV-Access Vascular Access Needle Guide Kit
• Version Model Number: 5432
• Catalog Number: 5432
• Company DUNS: 965417181
• Company Name: PROTEK MEDICAL PRODUCTS, INC.
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841912104697 [Primary]
GS1	10841912104694 [Package]; Contains: 00841912104697; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K973958

FDA Product Code

• ITX: Transducer, Ultrasonic, Diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-10-07
• Device Publish Date: 2017-01-06

On-Brand Devices [ProV-Access Vascular Access Needle Guide Kit]

• 10841912105714: 5415
• 10841912104694: 5432
• 10841912101440: 5431
• 10841912101433: 5430