AN22 - Andersen Miller-Abbott Type Intestinal Tube

GUDID 05060171440352

AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Individual)

ANDERSEN PRODUCTS, INC.

Nasogastric/orogastric tube

• Primary Device ID: 05060171440352
• NIH Device Record Key: bf542eee-29cd-4110-a6a6-54615c2d758f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AN22 - Andersen Miller-Abbott Type Intestinal Tube
• Version Model Number: AN22.00
• Company DUNS: 041867342
• Company Name: ANDERSEN 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060171440352 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011077

FDA Product Code

• KNT: Tubes, Gastrointestinal (And Accessories)

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: 2018-07-06
• Device Publish Date: 2017-01-24

On-Brand Devices [AN22 - Andersen Miller-Abbott Type Intestinal Tube]

• 05060171440581: AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Overpack 250 Ct.)
• 05060171440574: AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Case 50 Ct.)
• 05060171440567: AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Box 10 Ct.)
• 05060171440352: AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Individual)