Moss 5-17719

GUDID 00866459000400

Moss Gastrostomy Tube

MOSS TUBES, INC.

Gastrostomy tube

• Primary Device ID: 00866459000400
• NIH Device Record Key: 390806eb-1e18-4f46-b2a8-4184a86ef9ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Moss
• Version Model Number: 5-17719
• Catalog Number: 5-17719
• Company DUNS: 158510578
• Company Name: MOSS TUBES, 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)827-0470
• Email: mosstube@nycap.rr.com

Device Dimensions

• Catheter Gauge: 18 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00866459000400 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K990389

FDA Product Code

• KNT: TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Sterilization

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

[00866459000400]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-07
• Device Publish Date: 2017-10-04

On-Brand Devices [Moss]

• 00866459000417: Moss MarkIV Nasal Tube
• 00866459000400: Moss Gastrostomy Tube