Zammi 7510

GUDID 07899043000015

PRESSURE INFUSOR BAG - PREMERE 500 ML

Zammi Instrumental Eireli

Intravenous pressure infusor, manual, reusable

• Primary Device ID: 07899043000015
• NIH Device Record Key: e3b20f59-c51b-4880-b84d-5720ffbf42e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zammi
• Version Model Number: 7510
• Catalog Number: 7510
• Company DUNS: 898759832
• Company Name: Zammi Instrumental Eireli
• Device Count: 1
• 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: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07899043000015 [Primary]

FDA Product Code

• KZD: Infusor, Pressure, For I.V. Bags

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: 2023-03-21
• Device Publish Date: 2023-03-13

On-Brand Devices [Zammi]

• 07899043000053: ONE-WAY VALVE CHEST DRAINAGE SYSTEM - REPLACEMENT COLLECTION BAG PHYSIODRAIN 1000 ML
• 07899043000039: ONE-WAY VALVE CHEST DRAINAGE SYSTEM - PHYSIODRAIN 1000 ml
• 07899043000022: PRESSURE INFUSOR BAG - PREMERE 1000 ML
• 07899043000015: PRESSURE INFUSOR BAG - PREMERE 500 ML