Ameritus Oral Syringe AEG20-KMS-BA

GUDID 20817522013296

20ml oral syringe

KENTEC MEDICAL, INC.

Oral/enteral syringe, single-use

• Primary Device ID: 20817522013296
• NIH Device Record Key: 65815fc2-658a-4e8d-9d91-07095720f1c7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ameritus Oral Syringe
• Version Model Number: AEG20-KMS-BA
• Catalog Number: AEG20-KMS-BA
• Company DUNS: 066175613
• Company Name: KENTEC MEDICAL, INC.
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817522013292 [Unit of Use]
GS1	10817522013299 [Primary]
GS1	20817522013296 [Package]; Contains: 10817522013299; Package: box [200 Units]; In Commercial Distribution
GS1	30817522013293 [Package]; Package: case [800 Units]; In Commercial Distribution

FDA Product Code

• KYX: Dispenser, Liquid Medication

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: 2020-06-11
• Device Publish Date: 2020-06-03

On-Brand Devices [Ameritus Oral Syringe]

• 20817522013296: 20ml oral syringe
• 20817522013289: 10ml oral syringe
• 20817522013272: 5ml oral syringe
• 20817522013265: 3ml oral syringe
• 20817522013258: 1ml oral syringe