Navigator Aesthetic Delivery System NAV-038

GUDID 00851634007022

CARTICEPT MEDICAL, INC.

Infusion pump cassette

• Primary Device ID: 00851634007022
• NIH Device Record Key: 95ad600f-c0ec-4c39-817d-941da9761bd7
• Commercial Distribution Discontinuation: 2017-11-04
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Navigator Aesthetic Delivery System
• Version Model Number: NAV-038
• Catalog Number: NAV-038
• Company DUNS: 619025609
• Company Name: CARTICEPT MEDICAL, 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: false
• 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: 770-754-3800
• Email: info@carticept.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851634007015 [Primary]
GS1	00851634007022 [Package]; Contains: 00851634007015; Package: Case of 25 [25 Units]; Discontinued: 2017-11-04; Not in Commercial Distribution

FDA Product Code

• FRN: Pump, Infusion

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-17
• Device Publish Date: 2017-02-24

On-Brand Devices [Navigator Aesthetic Delivery System]

• 00851634007039: NAV-013
• 00851634007022: NAV-038
• 00851634007008: NAV-015